A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602543



Internal ID20975614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42352133..42354505hg38UCSC Ensembl
chr7:42391732..42394104hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg382373
hg192373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602543
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