A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615827



Internal ID20988898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2430623..2441793hg38UCSC Ensembl
chr7:2470258..2481428hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3811171
hg1911171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218419
Samples
Known GenesCHST12, LOC101927181
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615827
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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