A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6756n100



Internal ID20158372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:151033912..151093430hg38UCSC Ensembl
chr7:150730999..150790517hg19UCSC Ensembl
chr7:150361932..150421450hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3859519
hg1959519
hg1859519
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031733, nsv1028023
Samples
Known GenesABCB8, AGAP3, ASIC3, CDK5, FASTK, SLC4A2, TMUB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6756n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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