A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032130



Internal ID19121352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80862313..81012514hg38UCSC Ensembl
Innerchr6:81572030..81722231hg19UCSC Ensembl
Innerchr6:81628749..81778950hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38150202
hg19150202
hg18150202
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648864
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)nsv1032130
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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