A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880995



Internal ID22655966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214881165..214881225hg38UCSC Ensembl
chr1:215054508..215054568hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353190
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880995
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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