A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7771018



Internal ID13482181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10631054..10631055hg38UCSC Ensembl
Innerchr4:10631035..10631074hg38UCSC Ensembl
Outerchr4:10631034..10631075hg38UCSC Ensembl
chr4:10632678..10632679hg19UCSC Ensembl
Innerchr4:10632659..10632698hg19UCSC Ensembl
Outerchr4:10632658..10632699hg19UCSC Ensembl
chr4:10241776..10241777hg18UCSC Ensembl
Innerchr4:10241796..10241757hg18UCSC Ensembl
Outerchr4:10241756..10241797hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg386048
hg196048
hg186048
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3306200
Supporting Variants
SamplesNA12716
Known GenesCLNK
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7771018
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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