A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142999



Internal ID342200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:87631342..87631649hg38UCSC Ensembl
chr12:88025119..88025426hg19UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17689881
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142999
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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