A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963898



Internal ID18877863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29010183..29010254hg38UCSC Ensembl
Outerchr19:29501090..29501161hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129622
Supporting Variants
SamplesKWS1
Known GenesLOC100505835
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963898
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer