A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001804



Internal ID19190181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:15960310..15960569hg38UCSC Ensembl
Outerchr17:15863624..15863883hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150871
Supporting Variants
SamplesKWB1
Known GenesADORA2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001804
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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