A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999532



Internal ID19159069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75372007..75564011hg38UCSC Ensembl
Innerchr3:75421158..75613162hg19UCSC Ensembl
Innerchr3:75503848..75695852hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38192005
hg19192005
hg18192005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4777n100
Supporting Variantsnssv3594991
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999532
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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