A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432958



Internal ID21090511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81754389..81760004hg38UCSC Ensembl
chr8:82666624..82672239hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg385616
hg195616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171928
Samples
Known GenesCHMP4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432958
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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