A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006252



Internal ID18748783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6707783..7544588hg38UCSC Ensembl
Innerchr3:6749470..7586275hg19UCSC Ensembl
Innerchr3:6724470..7561275hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38836806
hg19836806
hg18836806
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591829
Samples
Known GenesGRM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006252
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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