A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2800435



Internal ID21245773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118263059..118263059hg38UCSC Ensembl
chr1:118805682..118805682hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13686508
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2800435
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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