A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326600



Internal ID20859737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156919252..156967851hg38UCSC Ensembl
chr1:156889044..156937643hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3848600
hg1948600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200931
Samples
Known GenesARHGEF11, LRRC71, MIR765
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326600
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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