A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010593



Internal ID19099810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36210223..36285997hg38UCSC Ensembl
Innerchr3:36251715..36327489hg19UCSC Ensembl
Innerchr3:36226719..36302493hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3875775
hg1975775
hg1875775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4718n100
Supporting Variantsnssv3589652
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)nsv1010593
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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