A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv97n137



Internal ID22812717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68691313..68691625hg38UCSC Ensembl
chr15:68983652..68983964hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv2795279, nsv2795483
Samples
Known GenesCORO2B
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)dgv97n137
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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