A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871866



Internal ID22646804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102488904..102489037hg38UCSC Ensembl
chr2:103105363..103105496hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399561
Samples
Known GenesSLC9A4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871866
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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