A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917870



Internal ID22693091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142256306..142256357hg38UCSC Ensembl
chr7:141956126..141956177hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445880
Samples
Known GenesPRSS58
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917870
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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