A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474644



Internal ID21132197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:84653332..84694619hg38UCSC Ensembl
chr12:85047111..85088398hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3841288
hg1941288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003957
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474644
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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