A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801703



Internal ID21247041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84756772..84756772hg38UCSC Ensembl
chr1:85222455..85222455hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13684998
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801703
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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