A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925576



Internal ID22700803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169771709..169771836hg38UCSC Ensembl
chr6:170171805..170171932hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409816
Samples
Known GenesERMARD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925576
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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