A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3469512



Internal ID19063422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:41916908..42000086hg38UCSC Ensembl
Innerchr1:42382579..42465757hg19UCSC Ensembl
Innerchr1:42155166..42238344hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3883179
hg1983179
hg1883179
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006768
Supporting Variants
Samples
Known GenesHIVEP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3469512
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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