A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506323



Internal ID22564269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36780635..36792991hg38UCSC Ensembl
chr7:36820240..36832596hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3812357
hg1912357
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846843
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506323
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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