A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795729



Internal ID21241067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1457329..1457428hg38UCSC Ensembl
chr16:1507330..1507429hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13681841
Samples
Known GenesCLCN7
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795729
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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