A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613523



Internal ID7000419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66832712..66840109hg38UCSC Ensembl
Innerchr7:66833212..66839609hg38UCSC Ensembl
Outerchr7:66831712..66841109hg38UCSC Ensembl
chr7:66297699..66305096hg19UCSC Ensembl
Innerchr7:66298199..66304596hg19UCSC Ensembl
Outerchr7:66296699..66306096hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg387398
hg197398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12819387
SamplesNA11881
Known GenesGTF2IRD1P1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613523
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