A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3596117



Internal ID18894398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75400451..75589578hg38UCSC Ensembl
Innerchr3:75449602..75638729hg19UCSC Ensembl
Innerchr3:75532292..75721419hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38189128
hg19189128
hg18189128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011531
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)nssv3596117
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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