A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141567



Internal ID340764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70206359..70215535hg38UCSC Ensembl
chr9:72821275..72830451hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg389177
hg199177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023290
Samples
Known GenesMAMDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141567
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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