A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448039



Internal ID21105592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75408001..75408600hg38UCSC Ensembl
chr10:77167759..77168358hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984054
Samples
Known GenesZNF503-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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