A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2815548



Internal ID21260886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138650778..138650778hg38UCSC Ensembl
chr7:138335523..138335523hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381275
hg191275
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13706845, nssv13706044
Samples
Known GenesSVOPL
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2815548
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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