A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2813573



Internal ID21258911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165839973..165839973hg38UCSC Ensembl
chr6:166253461..166253461hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13707567
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2813573
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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