A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496412



Internal ID20869614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55874737..55900912hg38UCSC Ensembl
chr15:56166935..56193110hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3826176
hg1926176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024867
Samples
Known GenesNEDD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496412
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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