A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602725



Internal ID20975796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30463200..30465690hg38UCSC Ensembl
chr7:30502816..30505306hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg382491
hg192491
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232510
Samples
Known GenesNOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602725
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