A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605858



Internal ID20978929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73612541..73615812hg38UCSC Ensembl
chr7:73026871..73030142hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383272
hg193272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159459
Samples
Known GenesMLXIPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605858
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