A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371652



Internal ID21029205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6958975..6966912hg38UCSC Ensembl
chr4:6960702..6968639hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg387938
hg197938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119012
Samples
Known GenesTBC1D14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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