A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891229



Internal ID18838939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:146522277..146792513hg38UCSC Ensembl
Outerchr7:146522277..146792513hg38UCSC Ensembl
Innerchr7:146219369..146489605hg19UCSC Ensembl
Outerchr7:146219369..146489605hg19UCSC Ensembl
Innerchr7:145850302..146120538hg18UCSC Ensembl
Outerchr7:145850302..146120538hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38270237
hg19270237
hg18270237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796878
Samples
Known GenesCNTNAP2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891229
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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