A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011770



Internal ID21921113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100150062..100150157hg38UCSC Ensembl
chr7:99747685..99747780hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560868
Samples
Known GenesLAMTOR4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011770
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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