A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910539



Internal ID22685750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157861863..157862615hg38UCSC Ensembl
chr7:157654555..157655307hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434855
Samples
Known GenesLOC100506585, PTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910539
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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