A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607377



Internal ID6647618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160656999..160657878hg38UCSC Ensembl
Innerchr5:160657015..160657863hg38UCSC Ensembl
Outerchr5:160656984..160657894hg38UCSC Ensembl
chr5:160084006..160084885hg19UCSC Ensembl
Innerchr5:160084022..160084870hg19UCSC Ensembl
Outerchr5:160083991..160084901hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38880
hg19880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12116544
SamplesHG03539
Known GenesATP10B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607377
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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