A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394112



Internal ID22451982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63140909..63234733hg38UCSC Ensembl
chr2:63368044..63461868hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3893825
hg1993825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885421
Supporting Variants
Samples
Known GenesWDPCP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394112
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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