A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1108973



Internal ID18936787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:87957187..87957246hg38UCSC Ensembl
Outerchr15:88500418..88500477hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3954778
SamplesKWS1
Known GenesNTRK3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1108973
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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