A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049115



Internal ID21958348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34992597..34992658hg38UCSC Ensembl
chr20:33580400..33580461hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635074
Samples
Known GenesMYH7B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049115
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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