A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604066



Internal ID20977137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169549251..169550680hg38UCSC Ensembl
chr6:169949347..169950776hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381430
hg191430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139934
Samples
Known GenesWDR27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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