A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468661



Internal ID21126214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:23563601..23564200hg38UCSC Ensembl
chr12:23716535..23717134hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998435
Samples
Known GenesSOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468661
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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