A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007551



Internal ID21916894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120892740..120930784hg38UCSC Ensembl
chr7:120532794..120570838hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3838045
hg1938045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564854
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007551
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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