A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960601



Internal ID18595849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41351014..41369437hg38UCSC Ensembl
Innerchr17:39507266..39525689hg19UCSC Ensembl
Innerchr17:36760792..36779215hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3818424
hg1918424
hg1818424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2761000, nssv2758259
SamplesHGDP01284, HGDP00927
Known GenesKRT33B
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960601
Frequency
Sample Size10
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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