A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028205



Internal ID19117423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:93932109..94075912hg38UCSC Ensembl
Innerchr6:94641827..94785630hg19UCSC Ensembl
Innerchr6:94698548..94842351hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38143804
hg19143804
hg18143804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648985
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)nsv1028205
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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