A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027683



Internal ID19116902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:81698469..81717138hg38UCSC Ensembl
Innerchr6:82408186..82426855hg19UCSC Ensembl
Innerchr6:82464905..82483574hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3818670
hg1918670
hg1818670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648872, nssv3648871
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027683
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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