A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561741



Internal ID21886096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41038845..41038981hg38UCSC Ensembl
chr7:41078443..41078579hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015342
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561741
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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