A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417529



Internal ID21075082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141581991..141584500hg38UCSC Ensembl
chr7:141281791..141284300hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg382510
hg192510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150770
Samples
Known GenesAGK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417529
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