A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003316



Internal ID21912659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90397502..90397682hg38UCSC Ensembl
chr7:90026816..90026996hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563260
Samples
Known GenesLOC101409256
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003316
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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