A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3465929



Internal ID19061483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72280838..72343056hg38UCSC Ensembl
Innerchr1:72746521..72808739hg19UCSC Ensembl
Innerchr1:72519109..72581327hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3862219
hg1962219
hg1862219
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998162
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)nssv3465929
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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