A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6169662



Internal ID9256586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141920665..141926712hg38UCSC Ensembl
chr7:141620465..141626512hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg386048
hg196048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2670563
Supporting Variants
SamplesNA12249
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6169662
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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