A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037088



Internal ID18779619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71582829..71827945hg38UCSC Ensembl
Innerchr11:71293875..71538991hg19UCSC Ensembl
Innerchr11:70971523..71216639hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38245117
hg19245117
hg18245117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1222n100
Supporting Variantsnssv3710642
Samples
Known GenesALG1L9P, FAM86C1, KRTAP5-11, ZNF705E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037088
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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