A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461203



Internal ID21118756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51208851..51209909hg38UCSC Ensembl
chr12:51602635..51603693hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg381059
hg191059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002135
Samples
Known GenesPOU6F1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461203
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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