A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613715



Internal ID6653924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74660298..74665599hg38UCSC Ensembl
Innerchr7:74660797..74665099hg38UCSC Ensembl
Outerchr7:74659298..74666598hg38UCSC Ensembl
chr7:74074628..74079931hg19UCSC Ensembl
Innerchr7:74075128..74079431hg19UCSC Ensembl
Outerchr7:74073628..74080931hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg385302
hg195304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12845475, essv12845476
SamplesHG02408, HG01800
Known GenesGTF2I
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613715
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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