A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3973393



Internal ID19244542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:11167036..11167241hg38UCSC Ensembl
Outerchr3:11208722..11208927hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1123624
Supporting Variants
SamplesKWS2
Known GenesHRH1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3973393
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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