A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489672



Internal ID21147225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25398157..25406025hg38UCSC Ensembl
chr13:25972295..25980163hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg387869
hg197869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008230
Samples
Known GenesATP8A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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