A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045088



Internal ID19134307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33309691..33538899hg38UCSC Ensembl
Innerchr11:33331237..33560445hg19UCSC Ensembl
Innerchr11:33287813..33517021hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38229209
hg19229209
hg18229209
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512711
Samples
Known GenesHIPK3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045088
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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