A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612659



Internal ID6999559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27497678..27507635hg38UCSC Ensembl
Innerchr7:27497691..27507622hg38UCSC Ensembl
Outerchr7:27497665..27507648hg38UCSC Ensembl
chr7:27537297..27547254hg19UCSC Ensembl
Innerchr7:27537310..27547241hg19UCSC Ensembl
Outerchr7:27537284..27547267hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg389958
hg199958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12713882
SamplesNA19792
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612659
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