A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133666



Internal ID19283970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:92836186..92837086hg38UCSC Ensembl
Outerchr7:92465500..92466400hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969234
SamplesKWS2
Known GenesCDK6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133666
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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