A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035558



Internal ID21944901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3231780..3237667hg38UCSC Ensembl
chr12:3340946..3346833hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg385888
hg195888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602959
Samples
Known GenesTSPAN9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035558
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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