A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533436



Internal ID20906797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:7071902..7078325hg38UCSC Ensembl
chr18:7071901..7078324hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg386424
hg196424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042757
Samples
Known GenesLAMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533436
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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