A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891231



Internal ID18838941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148175602..148186515hg38UCSC Ensembl
Outerchr7:148175413..148186516hg38UCSC Ensembl
Innerchr7:147872694..147883607hg19UCSC Ensembl
Outerchr7:147872505..147883608hg19UCSC Ensembl
Innerchr7:147503627..147514540hg18UCSC Ensembl
Outerchr7:147503438..147514541hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3811104
hg1911104
hg1811104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797686, essv25796779, essv25787143
Samples
Known GenesCNTNAP2, MIR548T
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891231
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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