A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455518



Internal ID21113071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118317964..118318654hg38UCSC Ensembl
chr10:120077476..120078166hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38691
hg19691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979549
Samples
Known GenesFAM204A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455518
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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