A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710767



Internal ID18662362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132032553..132083280hg38UCSC Ensembl
Innerchr11:131902447..131953174hg19UCSC Ensembl
Innerchr11:131407657..131458384hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3850728
hg1950728
hg1850728
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053895
Supporting Variants
Samples
Known GenesNTM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710767
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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