A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334027



Internal ID20867208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94185601..94186300hg38UCSC Ensembl
chr1:94651157..94651856hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065609
Samples
Known GenesARHGAP29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334027
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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