A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522700



Internal ID20896061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3136594..3137076hg38UCSC Ensembl
chr18:3136592..3137074hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039919
Samples
Known GenesMYOM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522700
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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