A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004715



Internal ID21914058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2485948..2486004hg38UCSC Ensembl
chr7:2525582..2525638hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559577
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004715
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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