A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961211



Internal ID19214465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:166416070..166416127hg38UCSC Ensembl
Outerchr6:166829558..166829615hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110802
Supporting Variants
SamplesKWS1
Known GenesRPS6KA2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961211
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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