A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14249671



Internal ID21302190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39158788..39283456hg38UCSC Ensembl
Outerchr9:39146321..39305149hg38UCSC Ensembl
Innerchr9:39158785..39283453hg19UCSC Ensembl
Outerchr9:39146318..39305146hg19UCSC Ensembl
Innerchr9:39148785..39273453hg18UCSC Ensembl
Outerchr9:39136318..39295146hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38158829
hg19158829
hg18158829
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169444
Supporting Variants
SamplesMLY_13
Known GenesCNTNAP3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14249671
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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