A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174615



Internal ID15526363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31467343..31674788hg38UCSC Ensembl
Innerchr11:31488890..31696336hg19UCSC Ensembl
Innerchr11:31445466..31652912hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38207446
hg19207447
hg18207447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553987
Supporting Variants
SamplesHGDP00106
Known GenesELP4, IMMP1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174615
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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