A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011893



Internal ID21921236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108257540..108417303hg38UCSC Ensembl
chr7:107897984..108057747hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38159764
hg19159764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569867
Samples
Known GenesNRCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011893
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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