A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032572



Internal ID18775106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110800096..111060820hg38UCSC Ensembl
Innerchr6:111121299..111382023hg19UCSC Ensembl
Innerchr6:111227992..111488716hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38260725
hg19260725
hg18260725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749512
Samples
Known GenesAMD1, CDK19, GSTM2P1, GTF3C6, RPF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032572
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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