A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501308



Internal ID22559246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134531043..134572778hg38UCSC Ensembl
chr7:134215795..134257530hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3841736
hg1941736
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856096
Supporting Variants
Samples
Known GenesAKR1B10, AKR1B15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501308
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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