A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558829



Internal ID21883184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130841089..130848772hg38UCSC Ensembl
chr7:130525848..130533531hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg387684
hg197684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002982
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558829
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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