A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021618



Internal ID19110836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137067419..137102642hg38UCSC Ensembl
Innerchr6:137388556..137423779hg19UCSC Ensembl
Innerchr6:137430249..137465472hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3835224
hg1935224
hg1835224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654412
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021618
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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