A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426543



Internal ID21084096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139480607..139546558hg38UCSC Ensembl
chr7:139165353..139231304hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3865952
hg1965952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233923
Samples
Known GenesCLEC2L, KLRG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426543
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