A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891228



Internal ID18838938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:146421002..146530532hg38UCSC Ensembl
Outerchr7:146421002..146530532hg38UCSC Ensembl
Innerchr7:146118094..146227624hg19UCSC Ensembl
Outerchr7:146118094..146227624hg19UCSC Ensembl
Innerchr7:145749027..145858557hg18UCSC Ensembl
Outerchr7:145749027..145858557hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38109531
hg19109531
hg18109531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784797
Samples
Known GenesCNTNAP2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891228
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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