A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122990



Internal ID19281583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:85513776..85515967hg38UCSC Ensembl
Outerchr15:86057007..86059198hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg382192
hg192192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970989, nssv3971586
SamplesKWS2, KWS1
Known GenesAKAP13
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122990
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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