A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035530



Internal ID21944873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95344317..95344609hg38UCSC Ensembl
chr12:95738093..95738385hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035530
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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