A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935197



Internal ID22710535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21091539..21091916hg38UCSC Ensembl
chr18:18671500..18671877hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370585
Samples
Known GenesROCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935197
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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