A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610862



Internal ID20983933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86342141..86377425hg38UCSC Ensembl
chr7:85971457..86006741hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3835285
hg1935285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159751
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610862
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