A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3974995



Internal ID18885326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:16266086..16266136hg38UCSC Ensembl
Outerchr6:16266317..16266367hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137067
Supporting Variants
SamplesKWS2
Known GenesGMPR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3974995
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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