A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037564



Internal ID21946907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101340937..101340988hg38UCSC Ensembl
chr12:101734715..101734766hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609983
Samples
Known GenesUTP20
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037564
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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