A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169403



Internal ID21313886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:126307627..127089515hg38UCSC Ensembl
Outerchr12:126295229..127091148hg38UCSC Ensembl
Innerchr12:126792173..127574060hg19UCSC Ensembl
Outerchr12:126779775..127575693hg19UCSC Ensembl
Innerchr12:125358126..126140013hg18UCSC Ensembl
Outerchr12:125345728..126141646hg18UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38795920
hg19795919
hg18795919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14241535
SamplesMLY_13
Known GenesLINC00943, LINC00944, LOC100128554, LOC101927592, LOC440117
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169403
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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