A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247629



Internal ID21302511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38203266..38325371hg38UCSC Ensembl
Outerchr11:38198170..38326560hg38UCSC Ensembl
Innerchr11:38224816..38346921hg19UCSC Ensembl
Outerchr11:38219720..38348110hg19UCSC Ensembl
Innerchr11:38181392..38303497hg18UCSC Ensembl
Outerchr11:38176296..38304686hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38128391
hg19128391
hg18128391
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169556
Supporting Variants
SamplesMLY_15
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247629
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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