A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501341



Internal ID22559279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137114523..137116195hg38UCSC Ensembl
chr7:136799270..136800942hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381673
hg191673
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848608
Supporting Variants
Samples
Known GenesLOC349160
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501341
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