A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6229n100



Internal ID22792316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3901571..3946771hg38UCSC Ensembl
chr7:3941203..3986403hg19UCSC Ensembl
chr7:3907729..3952929hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3845201
hg1945201
hg1845201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027500, nsv1020222, nsv1030082
Samples
Known GenesSDK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6229n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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