A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448085



Internal ID21105638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:64797372..65548152hg38UCSC Ensembl
chr10:66557129..67307910hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38750781
hg19750782
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195899
Samples
Known GenesANXA2P3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448085
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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