A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406292



Internal ID21063845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:137870158..137886400hg38UCSC Ensembl
chr5:137205847..137222089hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3816243
hg1916243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125309
Samples
Known GenesMYOT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406292
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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