A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006712



Internal ID21916055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108258391..108259607hg38UCSC Ensembl
chr7:107898835..107900051hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg381217
hg191217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561535
Samples
Known GenesNRCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006712
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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