A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970849



Internal ID19241213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:68415625..68415935hg38UCSC Ensembl
Outerchr11:68183093..68183403hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113405
Supporting Variants
SamplesKWS2
Known GenesLRP5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970849
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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