A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968709



Internal ID18900474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:93685836..93685900hg38UCSC Ensembl
Outerchr11:93419002..93419066hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113424
Supporting Variants
SamplesKWS2
Known GenesKIAA1731
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968709
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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