A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328767



Internal ID20861917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:174503301..174505200hg38UCSC Ensembl
chr1:174472439..174474338hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201051
Samples
Known GenesRABGAP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328767
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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