A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479358



Internal ID21136911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100615618..100616368hg38UCSC Ensembl
chr13:101267872..101268622hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38751
hg19751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006751
Samples
Known GenesTMTC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479358
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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