A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967335



Internal ID18883890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:184379812..184380512hg38UCSC Ensembl
Outerchr3:184097600..184098300hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112837
Supporting Variants
SamplesKWS2
Known GenesCHRD
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967335
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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