A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467885



Internal ID21125438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7763859..7870109hg38UCSC Ensembl
chr12:7916455..8022705hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38106251
hg19106251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004465
Samples
Known GenesNANOG, NANOGNB, SLC2A14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467885
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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