A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085707



Internal ID20652747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27500485..27509538hg38UCSC Ensembl
chr2:27723352..27732405hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg389054
hg199054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355265
Supporting Variants
Samples
Known GenesGCKR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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