A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501180



Internal ID22559117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:125342507..125347727hg38UCSC Ensembl
chr7:124982561..124987781hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg385221
hg195221
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852781
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501180
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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