A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13606252



Internal ID3608069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112634869..112691421hg38UCSC Ensembl
chr9:115397149..115453701hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3856553
hg1956553
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621518
Supporting Variants
SamplesNA20126
Known GenesINIP, KIAA1958
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13606252
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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