A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892774



Internal ID18836908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7142651..7182271hg38UCSC Ensembl
Outerchr16:7142651..7185946hg38UCSC Ensembl
Innerchr16:7192652..7232272hg19UCSC Ensembl
Outerchr16:7192652..7235947hg19UCSC Ensembl
Innerchr16:7132653..7172273hg18UCSC Ensembl
Outerchr16:7132653..7175948hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3843296
hg1943296
hg1843296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783587, essv25798205, essv25798807, essv25779572
Samples
Known GenesRBFOX1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892774
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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