A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005806



Internal ID21915149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45084230..45084347hg38UCSC Ensembl
chr7:45123829..45123946hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568288
Samples
Known GenesNACAD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005806
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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