A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021793



Internal ID19111011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:82010915..82027739hg38UCSC Ensembl
Innerchr6:82720632..82737456hg19UCSC Ensembl
Innerchr6:82777351..82794175hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3816825
hg1916825
hg1816825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6077n100
Supporting Variantsnssv3648878, nssv3648879, nssv3648877
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)nsv1021793
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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