A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085366



Internal ID20652406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:212166943..212178329hg38UCSC Ensembl
chr2:213031668..213043054hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3811387
hg1911387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354523
Supporting Variants
Samples
Known GenesERBB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085366
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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