A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027458



Internal ID21936801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29253226..29253280hg38UCSC Ensembl
chr12:29406159..29406213hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600291
Samples
Known GenesFAR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027458
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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