A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500794



Internal ID20874022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74721605..74745146hg38UCSC Ensembl
chr15:75013946..75037487hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3823542
hg1923542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026674
Samples
Known GenesCYP1A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500794
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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