A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111515



Internal ID19273164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:82882858..82888917hg38UCSC Ensembl
Outerchr15:83551610..83557669hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386060
hg196060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1256n106
Supporting Variantsnssv3963651
SamplesKWS2
Known GenesHOMER2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111515
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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