A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908124



Internal ID22683334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33211287..33211374hg38UCSC Ensembl
chr10:33500215..33500302hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357393
Samples
Known GenesNRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908124
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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