A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2815380



Internal ID21260718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7271947..7272266hg38UCSC Ensembl
chr6:7272180..7272499hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13698471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2815380
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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