A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022629



Internal ID18765163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:38159377..38249049hg38UCSC Ensembl
Innerchr8:38016895..38106567hg19UCSC Ensembl
Innerchr8:38136052..38225724hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3889673
hg1989673
hg1889673
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7162n100
Supporting Variantsnssv3685570
Samples
Known GenesBAG4, DDHD2, LSM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022629
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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