A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997946



Internal ID19157482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75366712..75666651hg38UCSC Ensembl
Innerchr3:75415863..75715802hg19UCSC Ensembl
Innerchr3:75498553..75798492hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38299940
hg19299940
hg18299940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3594962
Samples
Known GenesFAM86DP, FLJ20518, FRG2C, MIR1324
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997946
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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