A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509149



Internal ID20882456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26006901..26014400hg38UCSC Ensembl
chr15:26252048..26259547hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024303
Samples
Known GenesLOC100128714
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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