A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528596



Internal ID20901957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36918658..36990690hg38UCSC Ensembl
chr18:34498621..34570653hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3872033
hg1972033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039799
Samples
Known GenesKIAA1328
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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