A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060668



Internal ID19149887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41354648..41371051hg38UCSC Ensembl
Innerchr17:39510900..39527303hg19UCSC Ensembl
Innerchr17:36764426..36780829hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3816404
hg1916404
hg1816404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3173n100
Supporting Variantsnssv3545107
Samples
Known GenesKRT33B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060668
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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