A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033835



Internal ID18776368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12813166..12971126hg38UCSC Ensembl
Innerchr8:12670675..12828635hg19UCSC Ensembl
Innerchr8:12715046..12873006hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38157961
hg19157961
hg18157961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7083n100
Supporting Variantsnssv3666977
Samples
Known GenesKIAA1456, LINC00681
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033835
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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