A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019289



Internal ID21928632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58246258..58249858hg38UCSC Ensembl
chr10:60006019..60009619hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg383601
hg193601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586111
Samples
Known GenesIPMK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019289
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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