A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501316



Internal ID22559254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135099649..135100948hg38UCSC Ensembl
chr7:134784401..134785700hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850371
Supporting Variants
Samples
Known GenesAGBL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501316
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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