A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3594960



Internal ID18893241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75366712..75620267hg38UCSC Ensembl
Innerchr3:75415863..75669418hg19UCSC Ensembl
Innerchr3:75498553..75752108hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38253556
hg19253556
hg18253556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002163
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)nssv3594960
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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