A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3496581



Internal ID18737536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:179125436..179151145hg38UCSC Ensembl
Innerchr1:179094571..179120280hg19UCSC Ensembl
Innerchr1:177361194..177386903hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3825710
hg1925710
hg1825710
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012667
Supporting Variants
Samples
Known GenesABL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3496581
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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