A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11074006



Internal ID1075822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96617545..96628051hg38UCSC Ensembl
chr3:96336389..96346895hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3810507
hg1910507
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597075
Supporting Variants
SamplesHG03397
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11074006
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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