A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11765485



Internal ID1767301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:301153..312236hg38UCSC Ensembl
chr5:301268..312351hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3811084
hg1911084
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603740
Supporting Variants
SamplesHG00629
Known GenesAHRR, PDCD6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11765485
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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