A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3994477



Internal ID19216202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:62327601..62333501hg38UCSC Ensembl
Outerchr15:62619800..62625700hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg385901
hg195901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143782
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3994477
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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