A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499170



Internal ID20872387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56153780..56155601hg38UCSC Ensembl
chr15:56445978..56447799hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381822
hg191822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024875
Samples
Known GenesRFX7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499170
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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