A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438774



Internal ID21096327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18624051..18634084hg38UCSC Ensembl
chr10:18912980..18923013hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3810034
hg1910034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv636n223
Supporting Variantsnssv17980804
Samples
Known GenesNSUN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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