A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020108



Internal ID19109327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:119809968..120948547hg38UCSC Ensembl
Innerchr6:120131114..121269693hg19UCSC Ensembl
Innerchr6:120172813..121311392hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg381138580
hg191138580
hg181138580
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654337
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)nsv1020108
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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