A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15767456



Internal ID22101928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55237642..55237707hg38UCSC Ensembl
chr7:55305335..55305400hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4447093
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15767456
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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