A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970082



Internal ID19239717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35576450..35576507hg38UCSC Ensembl
Outerchr19:36067352..36067409hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1114001
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970082
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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