A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021789



Internal ID19111007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140703596..140963257hg38UCSC Ensembl
Innerchr6:141024733..141284394hg19UCSC Ensembl
Innerchr6:141066426..141326087hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38259662
hg19259662
hg18259662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654442
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)nsv1021789
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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