A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036854



Internal ID21946197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:59762276..59954882hg38UCSC Ensembl
chr12:60156057..60348663hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38192607
hg19192607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605765
Samples
Known GenesSLC16A7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036854
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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