A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3594990



Internal ID18893271
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 StatusS
Merged Variantsnsv1001019
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)nssv3594990
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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