A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6538n100



Internal ID20158154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102171110..103063688hg38UCSC Ensembl
chr7:101814390..102704135hg19UCSC Ensembl
chr7:101601110..102491371hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38892579
hg19889746
hg18890262
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016563, nsv1028438
Samples
Known GenesALKBH4, CUX1, FAM185A, FBXL13, LOC100289561, LOC100630923, LRRC17, LRWD1, MIR4285, MIR4467, MIR5090, ORAI2, POLR2J, POLR2J2, POLR2J3, PRKRIP1, RASA4, RASA4B, SH2B2, SPDYE2, SPDYE2B, SPDYE6, UPK3BL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6538n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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