A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002077



Internal ID18744608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41269871..41303354hg38UCSC Ensembl
Innerchr3:41311362..41344845hg19UCSC Ensembl
Innerchr3:41286366..41319849hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3833484
hg1933484
hg1833484
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589705
Samples
Known GenesULK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002077
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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