A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439750



Internal ID21097303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132341083..132400255hg38UCSC Ensembl
chr10:134154587..134213759hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3859173
hg1959173
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183334
Samples
Known GenesLRRC27, PWWP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439750
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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