A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970884



Internal ID18890539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:123087986..123088048hg38UCSC Ensembl
Outerchr11:122958694..122958756hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122675
Supporting Variants
SamplesKWS2
Known GenesCLMP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970884
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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