A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169752



Internal ID21313563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:47151419..47158633hg38UCSC Ensembl
Outerchr6:47148613..47158767hg38UCSC Ensembl
Innerchr6:47119155..47126369hg19UCSC Ensembl
Outerchr6:47116349..47126503hg19UCSC Ensembl
Innerchr6:47227114..47234328hg18UCSC Ensembl
Outerchr6:47224308..47234462hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3810155
hg1910155
hg1810155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245688
SamplesSNI_6
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169752
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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