A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795607



Internal ID21240945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81669286..81669376hg38UCSC Ensembl
chr16:81702891..81702981hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13703449
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795607
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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