A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3464398



Internal ID19060684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72280838..72346221hg38UCSC Ensembl
Innerchr1:72746521..72811904hg19UCSC Ensembl
Innerchr1:72519109..72584492hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3865384
hg1965384
hg1865384
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997734
Supporting Variants
Samples
Known GenesNEGR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3464398
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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