A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005614



Internal ID21914957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142010522..142012685hg38UCSC Ensembl
chr7:141710322..141712485hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg382164
hg192164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573087
Samples
Known GenesMGAM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005614
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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