A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876298



Internal ID22651258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119879641..119902331hg38UCSC Ensembl
chr1:120422264..120444954hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3822691
hg1922691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360461
Samples
Known GenesADAM30
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876298
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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