A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328205



Internal ID20861350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24076495..24076812hg38UCSC Ensembl
chr1:24402985..24403302hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060140
Samples
Known GenesMYOM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328205
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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