A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3954887



Internal ID19216787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:13962418..13962471hg38UCSC Ensembl
Outerchr17:13865735..13865788hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1109051
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3954887
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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