A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3733677



Internal ID19031958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75606908hg38UCSC Ensembl
Innerchr3:75427095..75656059hg19UCSC Ensembl
Innerchr3:75509785..75738749hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38228965
hg19228965
hg18228965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003210
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)nssv3733677
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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