A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461796



Internal ID239740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6719877..6733146hg38UCSC Ensembl
chr5:6719990..6733259hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3813270
hg1913270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961938
Samples
Known GenesPAPD7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461796
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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