A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030092



Internal ID19119311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:6396748..6497643hg38UCSC Ensembl
Innerchr6:6396981..6497876hg19UCSC Ensembl
Innerchr6:6341980..6442875hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38100896
hg19100896
hg18100896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654744
Samples
Known GenesLY86-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030092
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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