A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169962



Internal ID21314023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:124185122..124305084hg38UCSC Ensembl
Outerchr9:124182098..124305861hg38UCSC Ensembl
Innerchr9:126947401..127067363hg19UCSC Ensembl
Outerchr9:126944377..127068140hg19UCSC Ensembl
Innerchr9:125987222..126107184hg18UCSC Ensembl
Outerchr9:125984198..126107961hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38123764
hg19123764
hg18123764
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14251935
SamplesNGO_25
Known GenesNEK6
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169962
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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