A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959898



Internal ID18877903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:7077648..7077726hg38UCSC Ensembl
Outerchr17:6980967..6981045hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119455
Supporting Variants
SamplesKWS1
Known GenesCLEC10A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959898
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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