A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489897



Internal ID21147450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19243450..19710588hg38UCSC Ensembl
chr13:19817590..20284728hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38467139
hg19467139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007598
Samples
Known GenesANKRD26P3, LINC00421, MPHOSPH8, PSPC1, TPTE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489897
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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