A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496669



Internal ID20869872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49365218..49406687hg38UCSC Ensembl
chr15:49657415..49698884hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3841470
hg1941470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024778
Samples
Known GenesFAM227B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496669
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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