A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3992108



Internal ID19245837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:11482613..11482678hg38UCSC Ensembl
Outerchr6:11482846..11482911hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137065
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3992108
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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