A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530444



Internal ID20903805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3011501..3013500hg38UCSC Ensembl
chr18:3011499..3013498hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039674
Samples
Known GenesLPIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530444
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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