A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141968



Internal ID341168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39690000..39900000hg38UCSC Ensembl
chr9:41835018..42045018hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38210001
hg19210001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023002
Samples
Known GenesKGFLP2, LOC643648, MGC21881
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141968
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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