A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967734



Internal ID19245509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:66856929..66857229hg38UCSC Ensembl
Outerchr11:66624400..66624700hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131028
Supporting Variants
SamplesKWS2
Known GenesPC
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967734
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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