A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001305



Internal ID21910648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:11836178..11838965hg38UCSC Ensembl
chr7:11875804..11878591hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg382788
hg192788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567027
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001305
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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