A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795242



Internal ID21240580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45277841..45277986hg38UCSC Ensembl
chr15:45570039..45570184hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13691785
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795242
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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