A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032149



Internal ID19121371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:1847914..2005787hg38UCSC Ensembl
Innerchr6:1848148..2006021hg19UCSC Ensembl
Innerchr6:1793147..1951020hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38157874
hg19157874
hg18157874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3747899
Samples
Known GenesGMDS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032149
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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