A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002956



Internal ID19092173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96391359..96448851hg38UCSC Ensembl
Innerchr3:96110203..96167695hg19UCSC Ensembl
Innerchr3:97592893..97650385hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3857493
hg1957493
hg1857493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3735180
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002956
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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