A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589652



Internal ID18887933
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 StatusS
Merged Variantsnsv1010593
Supporting Variants
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)nssv3589652
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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