A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607319



Internal ID20980390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169525262..169632038hg38UCSC Ensembl
chr6:169925357..170032134hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38106777
hg19106778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139933
Samples
Known GenesWDR27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607319
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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