A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17440483



Internal ID22498353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23488945..23489128hg38UCSC Ensembl
chr7:23528564..23528747hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907745
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17440483
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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