A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489649



Internal ID21147202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:78839832..78842300hg38UCSC Ensembl
chr13:79413967..79416435hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg382469
hg192469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013060
Samples
Known GenesLINC00331
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489649
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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