A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025574



Internal ID21934917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102900100..102900300hg38UCSC Ensembl
chr12:103293878..103294078hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616749
Samples
Known GenesPAH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025574
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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