A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134442



Internal ID19254676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:44405800..44405874hg38UCSC Ensembl
Outerchr15:44697998..44698072hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3971937
SamplesKWS2
Known GenesCASC4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134442
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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