A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112280



Internal ID18903148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68400650..68400737hg38UCSC Ensembl
Outerchr15:68692989..68693076hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3965979
SamplesKWS2
Known GenesITGA11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112280
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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