A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016303



Internal ID21925646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65942850..65948480hg38UCSC Ensembl
chr5:65238678..65244308hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg385631
hg195631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546499
Samples
Known GenesERBB2IP, LOC100303749
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016303
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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