A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002702



Internal ID18745234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:35947159..36028350hg38UCSC Ensembl
Innerchr1:36412760..36493951hg19UCSC Ensembl
Innerchr1:36185347..36266538hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3881192
hg1981192
hg1881192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv149n100
Supporting Variantsnssv3465121
Samples
Known GenesAGO3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002702
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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