A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624715



Internal ID7011565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119774019..119780329hg38UCSC Ensembl
Innerchr10:119774019..119780329hg38UCSC Ensembl
Outerchr10:119773675..119780617hg38UCSC Ensembl
chr10:121533531..121539841hg19UCSC Ensembl
Innerchr10:121533531..121539841hg19UCSC Ensembl
Outerchr10:121533187..121540129hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg386311
hg196311
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13948148, essv13948139, essv13948140, essv13948141, essv13948147, essv13948142, essv13948146, essv13948145, essv13948143, essv13948149, essv13948144
SamplesHG03366, HG03521, HG03193, HG01198, NA19209, NA18871, HG03136, HG03388, HG01988, HG03077, HG03162
Known GenesINPP5F
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624715
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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