A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870906



Internal ID22645843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:73875073..73875707hg38UCSC Ensembl
chr2:74102200..74102834hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405353
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870906
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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