A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959913



Internal ID18862181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35105883..35105942hg38UCSC Ensembl
Outerchr19:35596787..35596846hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119470
Supporting Variants
SamplesKWS1
Known GenesHPN-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959913
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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