A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021200



Internal ID21930543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62817116..62817167hg38UCSC Ensembl
chr12:63210896..63210947hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615922
Samples
Known GenesPPM1H
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021200
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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