A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511998



Internal ID20885328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:33771501..34020300hg38UCSC Ensembl
chr15:34063702..34312501hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38248800
hg19248800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023598
Samples
Known GenesAVEN, CHRM5, RYR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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