A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603990



Internal ID20977061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119589201..119596000hg38UCSC Ensembl
chr7:119229255..119236054hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7098n223
Supporting Variantsnssv18151072
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603990
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