A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3577272



Internal ID18875553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:64690095..64832469hg38UCSC Ensembl
Innerchr2:64917229..65059603hg19UCSC Ensembl
Innerchr2:64770733..64913107hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38142375
hg19142375
hg18142375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003139
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3577272
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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