A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469835



Internal ID247612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157925244..157925967hg38UCSC Ensembl
chr6:158346276..158346999hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16990117
Samples
Known GenesSNX9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469835
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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