A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464269



Internal ID21121822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29043201..29054700hg38UCSC Ensembl
chr12:29196134..29207633hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3811500
hg1911500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464269
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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