A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1352e199



Internal ID22759125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75389229..75397426hg38UCSC Ensembl
chr9:78004145..78012342hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg388198
hg198198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2669464, esv2672196
SamplesNA11995, NA19914, HG00100, NA20531, HG01389, HG00151, HG00233, NA20532, NA12045, NA20805, NA12340, NA12058, HG01518, HG00261, HG01070, HG00272, HG01177, HG00173, NA20795, NA11992, NA20768, HG01083, NA20513, HG00158, HG00277, NA12275, HG01067, NA12156, HG00236, HG00262, NA12044, HG01440, HG01048, HG00326, HG01550, HG00253, HG00268, HG00282, NA19670, HG00145, HG00245, NA12342, NA12003, NA19788, HG00284, HG01073, HG00250, NA06989, HG01334, NA19761, HG00246, NA19675, NA12043, HG00258, NA20801, NA12716, HG00375, HG00136, HG00638, HG01357, NA20790, HG00237, NA19679, NA07037, NA06986, HG00339, HG00269, NA19785, HG00342, HG00310, NA20528, HG00372, HG00171, HG00345
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1352e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss74
Observed Complex0
Frequencyn/a


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