A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022754



Internal ID19111972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:154260863..154296376hg38UCSC Ensembl
Innerchr6:154581997..154617510hg19UCSC Ensembl
Innerchr6:154623689..154659202hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3835514
hg1935514
hg1835514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6165n100
Supporting Variantsnssv3654482
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)nsv1022754
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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