A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031231



Internal ID19120452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85764650..85837362hg38UCSC Ensembl
Innerchr6:86474368..86547080hg19UCSC Ensembl
Innerchr6:86531087..86603799hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3872713
hg1972713
hg1872713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6079n100
Supporting Variantsnssv3648896, nssv3750118, nssv3648897
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)nsv1031231
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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