A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17430272



Internal ID22488142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103155464..103155610hg38UCSC Ensembl
chr7:102795911..102796057hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925698
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17430272
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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