A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3391477



Internal ID15238444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2879192..2880390hg38UCSC Ensembl
Innerchr7:2879390..2880192hg38UCSC Ensembl
Outerchr7:2878192..2881390hg38UCSC Ensembl
chr7:2918826..2920024hg19UCSC Ensembl
Innerchr7:2919024..2919826hg19UCSC Ensembl
Outerchr7:2917826..2921024hg19UCSC Ensembl
chr7:2885352..2886550hg18UCSC Ensembl
Innerchr7:2886352..2885550hg18UCSC Ensembl
Outerchr7:2884352..2887550hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg381199
hg191199
hg181199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3740e59
Supporting Variantsessv8695770
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3391477
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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