A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006668



Internal ID19095885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75372007..75500783hg38UCSC Ensembl
Innerchr3:75421158..75549934hg19UCSC Ensembl
Innerchr3:75503848..75632624hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38128777
hg19128777
hg18128777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4774n100
Supporting Variantsnssv3594980, nssv3594977, nssv3594979, nssv3594976, nssv3732999, nssv3594978, nssv3732998
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)nsv1006668
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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