A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636575



Internal ID7023369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56155743..56156717hg38UCSC Ensembl
Innerchr15:56155749..56156711hg38UCSC Ensembl
Outerchr15:56155737..56156723hg38UCSC Ensembl
chr15:56447941..56448915hg19UCSC Ensembl
Innerchr15:56447947..56448909hg19UCSC Ensembl
Outerchr15:56447935..56448921hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38975
hg19975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15256393, essv15256410, essv15256399, essv15256409, essv15256413, essv15256394, essv15256391, essv15256406, essv15256398, essv15256401, essv15256400, essv15256412, essv15256403, essv15256395, essv15256397, essv15256407, essv15256402, essv15256396, essv15256411, essv15256408, essv15256404, essv15256405, essv15256392
SamplesHG03548, HG01140, HG03105, NA19457, NA19041, NA19137, NA20342, HG03169, HG02570, NA19210, HG03511, NA19318, HG03354, HG01190, NA18517, NA19712, HG03259, NA19323, HG03432, NA19438, HG01089, NA19030, NA19146
Known GenesRFX7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636575
Frequency
Sample Size2504
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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