A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032245



Internal ID21941588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27764934..27765065hg38UCSC Ensembl
chr12:27917867..27917998hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615716
Samples
Known GenesMANSC4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032245
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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