A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435738



Internal ID21093291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23312562..23319222hg38UCSC Ensembl
chr10:23601491..23608151hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg386661
hg196661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979718
Samples
Known GenesC10orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435738
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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