A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475136



Internal ID21132689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55650517..55656662hg38UCSC Ensembl
chr12:56044301..56050446hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg386146
hg196146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001801
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475136
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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