A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997914



Internal ID19157450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:207475081..207497283hg38UCSC Ensembl
Innerchr2:208339805..208362007hg19UCSC Ensembl
Innerchr2:208048050..208070252hg18UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3822203
hg1922203
hg1822203
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4155n100
Supporting Variantsnssv3585583
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)nsv997914
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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