A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3577292



Internal ID18875573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:71302364..71352283hg38UCSC Ensembl
Innerchr2:71529494..71579413hg19UCSC Ensembl
Innerchr2:71383002..71432921hg18UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg3849920
hg1949920
hg1849920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007844
Supporting Variants
Samples
Known GenesZNF638
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3577292
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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