A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17508865



Internal ID22566815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66216358..66218057hg38UCSC Ensembl
chr7:65681345..65683044hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848689
Supporting Variants
Samples
Known GenesTPST1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17508865
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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