A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014756



Internal ID21924099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73836200..73836396hg38UCSC Ensembl
chr7:73250530..73250726hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575882
Samples
Known GenesWBSCR27
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014756
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