A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510662



Internal ID20883983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71938001..71938900hg38UCSC Ensembl
chr15:72230342..72231241hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026437
Samples
Known GenesMYO9A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510662
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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