A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435576



Internal ID21093129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140061801..140063700hg38UCSC Ensembl
chr7:139761601..139763500hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224021
Samples
Known GenesPARP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435576
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer