A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006717



Internal ID19095935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75529695hg38UCSC Ensembl
Innerchr3:75427095..75578846hg19UCSC Ensembl
Innerchr3:75509785..75661536hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38151752
hg19151752
hg18151752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4776n100
Supporting Variantsnssv3602232, nssv3602231
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)nsv1006717
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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