A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500663



Internal ID20873891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27423727..27430111hg38UCSC Ensembl
chr15:27668873..27675257hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg386385
hg196385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023730
Samples
Known GenesGABRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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