A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15766915



Internal ID22101390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7432559..7432634hg38UCSC Ensembl
chr11:7453790..7453865hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4440905
Supporting Variants
Samples
Known GenesSYT9
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15766915
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