A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142591



Internal ID341792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63284862..63440862hg38UCSC Ensembl
chr9:67239834..67366296hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38156001
hg19126463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023082
Samples
Known GenesAQP7P1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142591
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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