A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959105



Internal ID19221714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:22745173..22763473hg38UCSC Ensembl
Outerchr17:22244500..22262800hg19UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg3818301
hg1918301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139672
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959105
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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