A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003222



Internal ID21912565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94604688..94604900hg38UCSC Ensembl
chr7:94234000..94234212hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576923
Samples
Known GenesSGCE
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003222
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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