A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702080



Internal ID15092046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:112708357..112715175hg38UCSC Ensembl
Innerchr10:114468116..114474934hg19UCSC Ensembl
Innerchr10:114458106..114464924hg18UCSC Ensembl
Innerchr10:114458106..114464924hg17UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg386819
hg196819
hg186819
hg176819
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525880
Supporting Variants
Samples
Known GenesVTI1A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702080
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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