A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035992



Internal ID21945335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30815640..30887390hg38UCSC Ensembl
chr15:31107843..31179593hg19UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3871751
hg1971751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606866
Samples
Known GenesHERC2P10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035992
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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