A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3596085



Internal ID18894366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75633155hg38UCSC Ensembl
Innerchr3:75427095..75682306hg19UCSC Ensembl
Innerchr3:75509785..75764996hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38255212
hg19255212
hg18255212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998064
Supporting Variants
Samples
Known GenesFAM86DP, MIR1324
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3596085
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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