A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011769



Internal ID19100987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:41920619..42006191hg38UCSC Ensembl
Innerchr1:42386290..42471862hg19UCSC Ensembl
Innerchr1:42158877..42244449hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3885573
hg1985573
hg1885573
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv156n100
Supporting Variantsnssv3471787
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)nsv1011769
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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