A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998222



Internal ID18843727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:67731276..67731519hg38UCSC Ensembl
Outerchr17:65727392..65727635hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146861
Supporting Variants
SamplesKWB1
Known GenesNOL11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998222
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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