A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615054



Internal ID20988125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18021035..18027902hg38UCSC Ensembl
chr7:18060658..18067525hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg386868
hg196868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154782
Samples
Known GenesPRPS1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615054
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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