A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613896



Internal ID20986967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45730517..45741460hg38UCSC Ensembl
chr7:45770116..45781059hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3810944
hg1910944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155077
Samples
Known GenesSEPT7P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613896
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