A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13690729



Internal ID21212582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150729220..150729567hg38UCSC Ensembl
chr1:150701696..150702043hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2800789
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13690729
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.392857


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