A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500670



Internal ID22558607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111072017..111085729hg38UCSC Ensembl
chr7:110712073..110725785hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3813713
hg1913713
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864233
Supporting Variants
Samples
Known GenesIMMP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500670
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