A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509062



Internal ID20882368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88522918..88523217hg38UCSC Ensembl
chr16:88589326..88589625hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033195
Samples
Known GenesZFPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509062
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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