A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501338



Internal ID22559276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137080402..137081874hg38UCSC Ensembl
chr7:136765149..136766621hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381473
hg191473
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866374
Supporting Variants
Samples
Known GenesLOC349160
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501338
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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