A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027155



Internal ID18769687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:38203999..38307554hg38UCSC Ensembl
Innerchr8:38061517..38165072hg19UCSC Ensembl
Innerchr8:38180674..38284229hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38103556
hg19103556
hg18103556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7164n100
Supporting Variantsnssv3685584
Samples
Known GenesBAG4, DDHD2, PPAPDC1B, WHSC1L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027155
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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