A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481270



Internal ID21138823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90924301..90934200hg38UCSC Ensembl
chr13:91576555..91586454hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg389900
hg199900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18014622
Samples
Known GenesLINC00410
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481270
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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