A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461835



Internal ID21119388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9859601..9860400hg38UCSC Ensembl
chr12:10012200..10012999hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006145
Samples
Known GenesCLEC2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461835
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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