A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394505



Internal ID22452375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:103436735..103441211hg38UCSC Ensembl
chr2:104053193..104057669hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg384477
hg194477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868701
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394505
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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