A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997844



Internal ID18848201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:7621058..7621601hg38UCSC Ensembl
Outerchr17:7524376..7524919hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152811
Supporting Variants
SamplesKWB1
Known GenesSHBG
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997844
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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