A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446754



Internal ID21104307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117011992..117039670hg38UCSC Ensembl
chr10:118771503..118799181hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3827679
hg1927679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978291
Samples
Known GenesKIAA1598
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446754
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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