A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488201



Internal ID21145754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51590825..51601116hg38UCSC Ensembl
chr13:52164961..52175252hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3810292
hg1910292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009687
Samples
Known GenesWDFY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488201
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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