A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891183



Internal ID19185579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111419830..111585090hg38UCSC Ensembl
Outerchr7:111252003..111711456hg38UCSC Ensembl
Innerchr7:111059886..111225146hg19UCSC Ensembl
Outerchr7:110892059..111351512hg19UCSC Ensembl
Innerchr7:110847122..111012382hg18UCSC Ensembl
Outerchr7:110679295..111138748hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38459454
hg19459454
hg18459454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799544, essv25785992, essv25797078, essv25800197, essv25782265, essv25797317, essv25779982, essv25786254
Samples
Known GenesIMMP2L
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891183
Frequency
Sample Size3017
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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