A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2815411



Internal ID21260749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87869373..87869373hg38UCSC Ensembl
chr6:88579091..88579091hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13703025
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2815411
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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