A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149686



Internal ID15878826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6189226..6232520hg38UCSC Ensembl
Innerchr17:6092546..6135840hg19UCSC Ensembl
Innerchr17:6033270..6076564hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3843295
hg1943295
hg1843295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574313
Supporting Variants
SamplesHGDP01264
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149686
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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