A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18078089



Internal ID20645129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143689106..143690109hg38UCSC Ensembl
chr2:144446675..144447678hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg381004
hg191004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343577
Supporting Variants
Samples
Known GenesARHGAP15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18078089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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