A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613517



Internal ID20986588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:117094641..117098926hg38UCSC Ensembl
chr7:116734695..116738980hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg384286
hg194286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148620
Samples
Known GenesST7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613517
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