A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636307



Internal ID7023103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44362810..44368089hg38UCSC Ensembl
Innerchr15:44362810..44368089hg38UCSC Ensembl
Outerchr15:44362310..44368589hg38UCSC Ensembl
chr15:44655008..44660287hg19UCSC Ensembl
Innerchr15:44655008..44660287hg19UCSC Ensembl
Outerchr15:44654508..44660787hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg385280
hg195280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15233231, essv15233232
SamplesHG01797, HG02113
Known GenesCASC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636307
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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