A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700651



Internal ID15090617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:107776457..108212812hg38UCSC Ensembl
Innerchr1:108319079..108755434hg19UCSC Ensembl
Innerchr1:108120602..108556957hg18UCSC Ensembl
Innerchr1:108031121..108467476hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38436356
hg19436356
hg18436356
hg17436356
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524680
Supporting Variants
Samples
Known GenesMIR7852, SLC25A24, VAV3, VAV3-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700651
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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