A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525915



Internal ID20899276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6867824..6873685hg38UCSC Ensembl
chr18:6867823..6873684hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg385862
hg195862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044651
Samples
Known GenesARHGAP28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525915
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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