A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957756



Internal ID18861000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:99376814..99376871hg38UCSC Ensembl
Outerchr6:99824690..99824747hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117658
Supporting Variants
SamplesKWS1
Known GenesCOQ3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957756
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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