A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121719



Internal ID19284682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:39361105..39365176hg38UCSC Ensembl
Outerchr15:39653306..39657377hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg384072
hg194072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968368
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121719
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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