A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434850



Internal ID22492720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43108227..43112297hg38UCSC Ensembl
chr7:43147826..43151896hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg384071
hg194071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923207
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434850
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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