A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12703863



Internal ID3672192
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612542
Supporting Variants
SamplesHG03270
Known GenesIGF2BP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12703863
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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