A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029193



Internal ID18771725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152091679..152135893hg38UCSC Ensembl
Innerchr6:152412814..152457028hg19UCSC Ensembl
Innerchr6:152454507..152498721hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3844215
hg1944215
hg1844215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749562
Samples
Known GenesESR1, SYNE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029193
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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