A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025426



Internal ID19114644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:11085419..11180394hg38UCSC Ensembl
Innerchr8:10942929..11037903hg19UCSC Ensembl
Innerchr8:10980339..11075313hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3894976
hg1994975
hg1894975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7013n100
Supporting Variantsnssv3681729
Samples
Known GenesXKR6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025426
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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