A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514219



Internal ID20887571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64602032..64604746hg38UCSC Ensembl
chr15:64894231..64896945hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382715
hg192715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025681
Samples
Known GenesZNF609
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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