A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600597



Internal ID6987639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57171668..57177179hg38UCSC Ensembl
Innerchr4:57171668..57177179hg38UCSC Ensembl
Outerchr4:57171507..57177373hg38UCSC Ensembl
chr4:58037834..58043345hg19UCSC Ensembl
Innerchr4:58037834..58043345hg19UCSC Ensembl
Outerchr4:58037673..58043539hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg385512
hg195512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11443252
SamplesHG02657
Known GenesIGFBP7-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600597
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer