A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705473



Internal ID15095439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47323088..47331763hg38UCSC Ensembl
Innerchr10:48407599..48416274hg19UCSC Ensembl
Innerchr10:48027605..48036280hg18UCSC Ensembl
Innerchr10:48027605..48036280hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg388676
hg198676
hg188676
hg178676
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528799
Supporting Variants
Samples
Known GenesGDF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705473
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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