A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142825



Internal ID342026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5930242..5945500hg38UCSC Ensembl
chr7:5969873..5985131hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3815259
hg1915259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16992537
Samples
Known GenesRSPH10B, RSPH10B2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142825
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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