A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507648



Internal ID20880942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72737008..72743443hg38UCSC Ensembl
chr15:73029349..73035784hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg386436
hg196436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026602
Samples
Known GenesBBS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507648
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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