A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449404



Internal ID22507274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149338048..149338204hg38UCSC Ensembl
chr7:149035139..149035295hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909716
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449404
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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