A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13764895



Internal ID3059288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44114009..44153040hg38UCSC Ensembl
Innerchr10:44114019..44153030hg38UCSC Ensembl
Outerchr10:44113999..44153050hg38UCSC Ensembl
chr10:44609457..44648488hg19UCSC Ensembl
Innerchr10:44609467..44648478hg19UCSC Ensembl
Outerchr10:44609447..44648498hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3839032
hg1939032
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623057
Supporting Variants
SamplesHG02688
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13764895
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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