A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701602



Internal ID15438254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:231062855..231171079hg38UCSC Ensembl
Innerchr2:231927569..232035793hg19UCSC Ensembl
Innerchr2:231635813..231744037hg18UCSC Ensembl
Innerchr2:231753074..231861298hg17UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38108225
hg19108225
hg18108225
hg17108225
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525474
Supporting Variants
Samples
Known GenesHTR2B, PSMD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701602
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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