A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13624968



Internal ID1254390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128760468..128766420hg38UCSC Ensembl
chr9:131522747..131528699hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg385953
hg195953
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621815
Supporting Variants
SamplesHG01107
Known GenesZER1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13624968
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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