A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3927561



Internal ID21347630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88616034..88616133hg38UCSC Ensembl
chr5:87911852..87911951hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15196370
SamplesHG002
Known GenesLINC00461
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3927561
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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