A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375148



Internal ID21032701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26650301..26657600hg38UCSC Ensembl
chr4:26651923..26659222hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg387300
hg197300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116135
Samples
Known GenesTBC1D19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375148
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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