A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959906



Internal ID19204941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:9057973..9058037hg38UCSC Ensembl
Outerchr18:9057971..9058035hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119463
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959906
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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