A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012040



Internal ID21921383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156942482..156957503hg38UCSC Ensembl
chr7:156735176..156750197hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3815022
hg1915022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562041
Samples
Known GenesNOM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012040
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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