A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602673



Internal ID20975744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37994954..39229437hg38UCSC Ensembl
chr7:38034556..39269036hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381234484
hg191234481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156463
Samples
Known GenesAMPH, FAM183B, POU6F2, STARD3NL, TARP, TRG-AS1, VPS41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602673
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