A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2761000



Internal ID17825172
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv960601
Supporting Variants
SamplesHGDP00927
Known GenesKRT33B
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2761000
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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