A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13031687



Internal ID2510869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154822691..154824967hg38UCSC Ensembl
Innerchr7:154822701..154824957hg38UCSC Ensembl
Outerchr7:154822681..154824977hg38UCSC Ensembl
chr7:154614401..154616677hg19UCSC Ensembl
Innerchr7:154614411..154616667hg19UCSC Ensembl
Outerchr7:154614391..154616687hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg382277
hg192277
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615616
Supporting Variants
SamplesHG02230
Known GenesDPP6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13031687
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