A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013196



Internal ID19102414
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 StatusM
Merged Variantsdgv4777n100
Supporting Variantsnssv3601992, nssv3601989, nssv3601990, nssv3601991
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)nsv1013196
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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