A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636580



Internal ID6676687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56250978..56252789hg38UCSC Ensembl
Innerchr15:56251006..56252761hg38UCSC Ensembl
Outerchr15:56250950..56252817hg38UCSC Ensembl
chr15:56543176..56544987hg19UCSC Ensembl
Innerchr15:56543204..56544959hg19UCSC Ensembl
Outerchr15:56543148..56545015hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381812
hg191812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15256438, essv15256439, essv15256437, essv15256436
SamplesHG00121, HG01465, HG01524, HG00101
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636580
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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