A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480971



Internal ID21138524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97977001..97984300hg38UCSC Ensembl
chr13:98629255..98636554hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg387300
hg197300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192136
Samples
Known GenesIPO5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480971
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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