A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14242523



Internal ID21302383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126112035..126200187hg38UCSC Ensembl
Outerchr9:126108555..126203830hg38UCSC Ensembl
Innerchr9:128874314..128962466hg19UCSC Ensembl
Outerchr9:128870834..128966109hg19UCSC Ensembl
Innerchr9:127914135..128002287hg18UCSC Ensembl
Outerchr9:127910655..128005930hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3895276
hg1995276
hg1895276
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169798
Supporting Variants
SamplesMLY_14
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14242523
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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