A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614730



Internal ID7001623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:118239408..118268273hg38UCSC Ensembl
Innerchr7:118239422..118268260hg38UCSC Ensembl
Outerchr7:118239395..118268287hg38UCSC Ensembl
chr7:117879462..117908327hg19UCSC Ensembl
Innerchr7:117879476..117908314hg19UCSC Ensembl
Outerchr7:117879449..117908341hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3828866
hg1928866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12938481
SamplesHG03478
Known GenesANKRD7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614730
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