A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610436



Internal ID20983507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114459248..114475769hg38UCSC Ensembl
chr7:114099303..114115824hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3816522
hg1916522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149280
Samples
Known GenesFOXP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610436
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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