A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961120



Internal ID19209168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:51831622..51831711hg38UCSC Ensembl
Outerchr17:49908982..49909071hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110712
Supporting Variants
SamplesKWS1
Known GenesCA10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961120
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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