A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8696532



Internal ID15058261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130777644..130778342hg38UCSC Ensembl
Innerchr9:130777643..130778343hg38UCSC Ensembl
Outerchr9:130776644..130779342hg38UCSC Ensembl
chr9:133653031..133653729hg19UCSC Ensembl
Innerchr9:133653030..133653730hg19UCSC Ensembl
Outerchr9:133652031..133654729hg19UCSC Ensembl
chr9:132642852..132643550hg18UCSC Ensembl
Innerchr9:132643551..132642851hg18UCSC Ensembl
Outerchr9:132641852..132644550hg18UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg38699
hg19699
hg18699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3396177
Supporting Variants
SamplesNA19239
Known GenesABL1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8696532
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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