A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000807



Internal ID21910150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108043547..108043598hg38UCSC Ensembl
chr7:107683992..107684043hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568097
Samples
Known GenesLAMB4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000807
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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