A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662594



Internal ID9928699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9757025..9757488hg38UCSC Ensembl
chr1:9817083..9817546hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6434280, essv6053227, essv6552130, essv5605258
SamplesHG01072, HG00133, NA11893, HG00319
Known GenesCLSTN1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662594
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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