A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872713



Internal ID22647654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77569931..77602562hg38UCSC Ensembl
chr2:77797057..77829688hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3832632
hg1932632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404580
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872713
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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