A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984357



Internal ID19205085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93874469..93880102hg38UCSC Ensembl
Outerchr11:93607635..93613268hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg385634
hg195634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112495
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984357
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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