A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990952



Internal ID19227170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:75088197..75088269hg38UCSC Ensembl
Outerchr15:75380538..75380610hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1138387
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990952
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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