A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13606581



Internal ID2809009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113040467..113063600hg38UCSC Ensembl
chr9:115802747..115825880hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3823134
hg1923134
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621527
Supporting Variants
SamplesHG02481
Known GenesZFP37
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13606581
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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