A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978859



Internal ID18892343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35105883..35105938hg38UCSC Ensembl
Outerchr19:35596787..35596842hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140147
Supporting Variants
SamplesKWS2
Known GenesHPN-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978859
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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