A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952078



Internal ID16954265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89602793..89640192hg38UCSC Ensembl
Outerchr16:89669201..89706600hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3837400
hg1937400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000197
SamplesBILGI_BIOE
Known GenesDPEP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952078
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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