A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001097



Internal ID19090314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75379820..75537642hg38UCSC Ensembl
Innerchr3:75428971..75586793hg19UCSC Ensembl
Innerchr3:75511661..75669483hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38157823
hg19157823
hg18157823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4776n100
Supporting Variantsnssv3596093
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)nsv1001097
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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