A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431311



Internal ID22489181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92597982..92599027hg38UCSC Ensembl
chr7:92227296..92228341hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg381046
hg191046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912681
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431311
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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