A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503634



Internal ID20876890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71954637..71978979hg38UCSC Ensembl
chr15:72246978..72271320hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3824343
hg1924343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026557
Samples
Known GenesMYO9A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503634
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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