A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437935



Internal ID21095488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23222110..23225663hg38UCSC Ensembl
chr10:23511039..23514592hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg383554
hg193554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979712
Samples
Known GenesC10orf115
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437935
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer