A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014559



Internal ID21923902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92146666..92146823hg38UCSC Ensembl
chr7:91775980..91776137hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568805
Samples
Known GenesLRRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014559
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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