A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019332



Internal ID21928675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129809970..129810049hg38UCSC Ensembl
chr7:129449810..129449889hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564674
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019332
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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