A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131202



Internal ID19259750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:74936054..74936122hg38UCSC Ensembl
Outerchr15:75228395..75228463hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970981
SamplesKWS1
Known GenesCOX5A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131202
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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