A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005725



Internal ID19094942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75608958hg38UCSC Ensembl
Innerchr3:75427095..75658109hg19UCSC Ensembl
Innerchr3:75509785..75740799hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38231015
hg19231015
hg18231015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4777n100
Supporting Variantsnssv3733682, nssv3733680, nssv3733683, nssv3733681, nssv3596079, nssv3596078, nssv3596077
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)nsv1005725
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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