A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3601989



Internal ID18900270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75372007..75608958hg38UCSC Ensembl
Innerchr3:75421158..75658109hg19UCSC Ensembl
Innerchr3:75503848..75740799hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38236952
hg19236952
hg18236952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013196
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)nssv3601989
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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