A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516281



Internal ID20889642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9434926..9436202hg38UCSC Ensembl
chr18:9434924..9436200hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381277
hg191277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516281
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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