A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619239



Internal ID20992310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:115637501..115662300hg38UCSC Ensembl
chr7:115277555..115302354hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3824800
hg1924800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7094n223
Supporting Variantsnssv18233228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619239
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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