A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035141



Internal ID21944484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90235743..90237136hg38UCSC Ensembl
chr15:90778975..90780368hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381394
hg191394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610012
Samples
Known GenesCIB1, GDPGP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035141
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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