A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5684377



Internal ID8661780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121461003..121468865hg38UCSC Ensembl
Outerchr9:121460966..121468915hg38UCSC Ensembl
Innerchr9:124223281..124231143hg19UCSC Ensembl
Outerchr9:124223244..124231193hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg387950
hg197950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2668147
Supporting Variants
SamplesNA19138
Known GenesGGTA1P
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5684377
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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