A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022072



Internal ID18764606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10374492..10581628hg38UCSC Ensembl
Innerchr6:10374725..10581861hg19UCSC Ensembl
Innerchr6:10482711..10689847hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38207137
hg19207137
hg18207137
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654764
Samples
Known GenesGCNT2, LINC00518, MIR5689, TFAP2A, TFAP2A-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022072
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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