A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570268



Internal ID21762311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:118642500..118781470hg38UCSC Ensembl
chr7:118282554..118421524hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38138971
hg19138971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001818
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570268
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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