A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490855



Internal ID21148408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51397359..51397780hg38UCSC Ensembl
chr13:51971495..51971916hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009671
Samples
Known GenesINTS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490855
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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