A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572960



Internal ID21521356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74369856..74370154hg38UCSC Ensembl
chr7:73784186..73784484hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142029
SamplesHG00731
Known GenesCLIP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572960
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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