A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326186



Internal ID20859320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:174340452..174356227hg38UCSC Ensembl
chr1:174309590..174325365hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3815776
hg1915776
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201044
Samples
Known GenesRABGAP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326186
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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