A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001352



Internal ID19090569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:41933839..42000086hg38UCSC Ensembl
Innerchr1:42399510..42465757hg19UCSC Ensembl
Innerchr1:42172097..42238344hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3866248
hg1966248
hg1866248
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv156n100
Supporting Variantsnssv3465671
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)nsv1001352
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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