A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461071



Internal ID21118624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:73741556..73741920hg38UCSC Ensembl
chr12:74135336..74135700hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002746
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461071
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer