A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8936613



Internal ID14962770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95635459..95635477hg38UCSC Ensembl
Innerchr7:95635463..95635471hg38UCSC Ensembl
Outerchr7:95635447..95635489hg38UCSC Ensembl
chr7:95264771..95264789hg19UCSC Ensembl
Innerchr7:95264775..95264783hg19UCSC Ensembl
Outerchr7:95264759..95264801hg19UCSC Ensembl
chr7:95102707..95102725hg18UCSC Ensembl
Innerchr7:95102719..95102711hg18UCSC Ensembl
Outerchr7:95102695..95102737hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38251
hg19251
hg18251
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3330424
Supporting Variants
SamplesNA19190
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8936613
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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