A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2804629



Internal ID21249967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32331002..32331002hg38UCSC Ensembl
chr22:32726989..32726989hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13694916
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2804629
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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