A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507619



Internal ID20880913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31025101..31037621hg38UCSC Ensembl
chr16:31036422..31048942hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3812521
hg1912521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028922
Samples
Known GenesSTX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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