A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008006



Internal ID21917349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66065591..66065645hg38UCSC Ensembl
chr5:65361419..65361473hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539309
Samples
Known GenesERBB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008006
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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