A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017551



Internal ID19106768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110063851..110092022hg38UCSC Ensembl
Innerchr6:110385054..110413225hg19UCSC Ensembl
Innerchr6:110491747..110519918hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3828172
hg1928172
hg1828172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6136n100
Supporting Variantsnssv3654287
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)nsv1017551
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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