A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151421



Internal ID19201910
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 StatusM
Merged Variants
Supporting Variantsnssv4003985
SamplesKWB1
Known GenesNXN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151421
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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