A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610937



Internal ID20984008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83417422..83418037hg38UCSC Ensembl
chr7:83046738..83047353hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161004
Samples
Known GenesSEMA3E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610937
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