A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028225



Internal ID19117443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94746243..94924579hg38UCSC Ensembl
Innerchr6:95455961..95634297hg19UCSC Ensembl
Innerchr6:95512682..95691018hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38178337
hg19178337
hg18178337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6101n100
Supporting Variantsnssv3649031
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)nsv1028225
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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