A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602545



Internal ID20975616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93811345..93985532hg38UCSC Ensembl
chr7:93440657..93614844hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38174188
hg19174188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162037
Samples
Known GenesGNG11, GNGT1, TFPI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602545
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