A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437797



Internal ID21095350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26579164..26637493hg38UCSC Ensembl
chr10:26868093..26926422hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3858330
hg1958330
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv662n223
Supporting Variantsnssv18180243
Samples
Known GenesLINC00264
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437797
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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