A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061557



Internal ID19150776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41348341..41370045hg38UCSC Ensembl
Innerchr17:39504593..39526297hg19UCSC Ensembl
Innerchr17:36758119..36779823hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3821705
hg1921705
hg1821705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3171n100
Supporting Variantsnssv3544205
Samples
Known GenesKRT33A, KRT33B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061557
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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