A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498664



Internal ID20871877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84699592..84700770hg38UCSC Ensembl
chr15:85242823..85244001hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg381179
hg191179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027230
Samples
Known GenesSEC11A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498664
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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