A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450051



Internal ID21107604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37770436..37780330hg38UCSC Ensembl
chr10:38059364..38069258hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg389895
hg199895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979931
Samples
Known GenesZNF248
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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