A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017821



Internal ID21927164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71387214..71387277hg38UCSC Ensembl
chr7:70852200..70852263hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572884
Samples
Known GenesWBSCR17
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017821
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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