A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915732



Internal ID22690950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99219897..99375922hg38UCSC Ensembl
chr7:98817520..98973545hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38156026
hg19156026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434691
Samples
Known GenesARPC1A, ARPC1B, MYH16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915732
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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