A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612542



Internal ID6999443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23370770..23372276hg38UCSC Ensembl
Innerchr7:23370770..23372276hg38UCSC Ensembl
Outerchr7:23370621..23372396hg38UCSC Ensembl
chr7:23410389..23411895hg19UCSC Ensembl
Innerchr7:23410389..23411895hg19UCSC Ensembl
Outerchr7:23410240..23412015hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381507
hg191507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12703864, essv12703863
SamplesNA19704, HG03270
Known GenesIGF2BP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612542
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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