A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506387



Internal ID22564334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38359276..38361666hg38UCSC Ensembl
chr7:38398877..38401267hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg382391
hg192391
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846339
Supporting Variants
Samples
Known GenesTRG-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506387
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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