A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442521



Internal ID21100074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30924303..30931761hg38UCSC Ensembl
chr10:31213232..31220690hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg387459
hg197459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981422
Samples
Known GenesZNF438
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442521
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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