A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354191



Internal ID21011744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143250801..143255500hg38UCSC Ensembl
chr2:144008370..144013069hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077754
Samples
Known GenesARHGAP15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354191
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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