A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419639



Internal ID21077192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81757911..81766709hg38UCSC Ensembl
chr8:82670146..82678944hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg388799
hg198799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171929
Samples
Known GenesCHMP4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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