A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737966



Internal ID20513931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22977877..22984277hg38UCSC Ensembl
chr7:23017496..23023896hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg386401
hg196401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275828
Samples
Known GenesFAM126A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737966
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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