A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3730851



Internal ID19029132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:60147758..60182291hg38UCSC Ensembl
Innerchr2:60374893..60409426hg19UCSC Ensembl
Innerchr2:60228397..60262930hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3834534
hg1934534
hg1834534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009051
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)nssv3730851
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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