A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444897



Internal ID21102450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43463172..43468675hg38UCSC Ensembl
chr10:43958620..43964123hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg385504
hg195504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981653
Samples
Known GenesZNF487
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444897
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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