A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247627



Internal ID21311827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76941965..76944420hg38UCSC Ensembl
Outerchr9:76939544..76951948hg38UCSC Ensembl
Innerchr9:79556881..79559336hg19UCSC Ensembl
Outerchr9:79554460..79566864hg19UCSC Ensembl
Innerchr9:78746701..78749156hg18UCSC Ensembl
Outerchr9:78744280..78756684hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3812405
hg1912405
hg1812405
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169957
Supporting Variants
SamplesSNI_13
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247627
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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