A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601993



Internal ID20975064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151396753..151418289hg38UCSC Ensembl
chr6:151717888..151739424hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3821537
hg1921537
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217118
Samples
Known GenesRMND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601993
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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