A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390088



Internal ID21381223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:181908866..181909533hg38UCSC Ensembl
chr2:182773593..182774260hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38668
hg19668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706889
Samples
Known GenesSSFA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390088
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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