A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020567



Internal ID21929910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39703778..39704228hg38UCSC Ensembl
chr17:37860031..37860481hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622599
Samples
Known GenesERBB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020567
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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