A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170284



Internal ID21314345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153620648..153658366hg38UCSC Ensembl
Outerchr6:153616611..153659377hg38UCSC Ensembl
Innerchr6:153941783..153979501hg19UCSC Ensembl
Outerchr6:153937746..153980512hg19UCSC Ensembl
Innerchr6:153983476..154021194hg18UCSC Ensembl
Outerchr6:153979439..154022205hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3842767
hg1942767
hg1842767
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244963, nssv14250201
SamplesNGO_37, SNI_6
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170284
Frequency
Sample Size93
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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