A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18075596



Internal ID20642636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11336501..11337900hg38UCSC Ensembl
chr2:11476627..11478026hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6347832
Supporting Variants
Samples
Known GenesROCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18075596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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