A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003985



Internal ID19189358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:914180..914316hg38UCSC Ensembl
Outerchr17:817420..817556hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151421
Supporting Variants
SamplesKWB1
Known GenesNXN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003985
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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