A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609913



Internal ID20982984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119397901..119434200hg38UCSC Ensembl
chr7:119037955..119074254hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3836300
hg1936300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7096n223
Supporting Variantsnssv18219901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609913
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer