A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458932



Internal ID22516813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61149705..61168687hg38UCSC Ensembl
chr11:60917177..60936159hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3818983
hg1918983
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851238
Supporting Variants
Samples
Known GenesVPS37C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458932
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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