A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15765967



Internal ID22100438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44662965..44663779hg38UCSC Ensembl
chr11:44684515..44685329hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38815
hg19815
Variant TypeOTHER delins
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4445822
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SUBSINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15765967
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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