A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395270



Internal ID22453140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102887961..102888124hg38UCSC Ensembl
chr2:103504420..103504583hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880667
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395270
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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