A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871003



Internal ID22645941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40109765..40121693hg38UCSC Ensembl
chr1:40575437..40587365hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3811929
hg1911929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382724
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871003
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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