A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3594938



Internal ID18893219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75366712..75571732hg38UCSC Ensembl
Innerchr3:75415863..75620883hg19UCSC Ensembl
Innerchr3:75498553..75703573hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38205021
hg19205021
hg18205021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999685
Supporting Variants
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)nssv3594938
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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