A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413069



Internal ID21070622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:127072701..127076200hg38UCSC Ensembl
chr5:126408393..126411892hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213193
Samples
Known GenesC5orf63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413069
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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