A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730923



Internal ID20506839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:785200..785277hg38UCSC Ensembl
chr7:824837..824914hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262231
Samples
Known GenesHEATR2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730923
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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