A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985528



Internal ID18864985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:14326764..14327080hg38UCSC Ensembl
Outerchr11:14348310..14348626hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122585
Supporting Variants
SamplesKWS1
Known GenesRRAS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985528
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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