A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437321



Internal ID21094874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126457401..126466018hg38UCSC Ensembl
chr10:128145970..128154587hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg388618
hg198618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978681
Samples
Known GenesC10orf90
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437321
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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