A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002420



Internal ID21911763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38459218..38460618hg38UCSC Ensembl
chr7:38498818..38500218hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381401
hg191401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573141
Samples
Known GenesAMPH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002420
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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