A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3972665



Internal ID19232447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:27240939..27241108hg38UCSC Ensembl
Outerchr19:27731847..27732016hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134779
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3972665
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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