A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990967



Internal ID19241588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:92748864..92748941hg38UCSC Ensembl
Outerchr15:93292094..93292171hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113733
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990967
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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