A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967841



Internal ID18883832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:37489794..37490194hg38UCSC Ensembl
Outerchr17:35849900..35850300hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136235
Supporting Variants
SamplesKWS2
Known GenesDUSP14
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967841
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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