A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3501322



Internal ID19088963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:153699555..153746270hg38UCSC Ensembl
Innerchr1:153672031..153718746hg19UCSC Ensembl
Innerchr1:151938655..151985370hg18UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3846716
hg1946716
hg1846716
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002328
Supporting Variants
Samples
Known GenesINTS3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3501322
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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