A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025093



Internal ID19114311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:154257211..154296376hg38UCSC Ensembl
Innerchr6:154578345..154617510hg19UCSC Ensembl
Innerchr6:154620037..154659202hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3839166
hg1939166
hg1839166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6165n100
Supporting Variantsnssv3654481
Samples
Known GenesIPCEF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025093
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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