A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022025



Internal ID18764559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:38199815..38249049hg38UCSC Ensembl
Innerchr8:38057333..38106567hg19UCSC Ensembl
Innerchr8:38176490..38225724hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3849235
hg1949235
hg1849235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7163n100
Supporting Variantsnssv3685576, nssv3685579, nssv3685575, nssv3685573, nssv3685577, nssv3685578, nssv3685574
Samples
Known GenesBAG4, DDHD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022025
Frequency
Sample Size29084
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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