A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981469



Internal ID19215703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:18433490..18434090hg38UCSC Ensembl
Outerchr19:18544300..18544900hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1144870
Supporting Variants
SamplesKWS1
Known GenesSSBP4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981469
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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