A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15760788



Internal ID22095279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6551814..6552262hg38UCSC Ensembl
chr11:6573044..6573492hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4440901
Supporting Variants
Samples
Known GenesDNHD1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15760788
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