A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001019



Internal ID19090236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75372007..75559476hg38UCSC Ensembl
Innerchr3:75421158..75608627hg19UCSC Ensembl
Innerchr3:75503848..75691317hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38187470
hg19187470
hg18187470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4777n100
Supporting Variantsnssv3594990
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)nsv1001019
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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