A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453848



Internal ID21111401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26072805..26155913hg38UCSC Ensembl
chr10:26361734..26444842hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3883109
hg1983109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981152
Samples
Known GenesMYO3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453848
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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