A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028023



Internal ID18770554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:151041537..151093430hg38UCSC Ensembl
Innerchr7:150738624..150790517hg19UCSC Ensembl
Innerchr7:150369557..150421450hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3851894
hg1951894
hg1851894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6756n100
Supporting Variantsnssv3757726, nssv3757725
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)nsv1028023
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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