A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677004



Internal ID9943109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129340328..129340558hg38UCSC Ensembl
Outerchr9:129340289..129340615hg38UCSC Ensembl
Innerchr9:132102607..132102837hg19UCSC Ensembl
Outerchr9:132102568..132102894hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5559599, essv6180352, essv6016202, essv6121837, essv5764944, essv6453630, essv6400979, essv6300315, essv5939602, essv5884604, essv5753486, essv6005796, essv6585772, essv6336809, essv6523409, essv6447643, essv5676691, essv5495828
SamplesNA19457, NA18874, HG00236, NA19075, NA18520, NA18985, HG00264, NA11831, NA12342, HG00146, NA18541, HG00124, NA12272, NA19472, NA19779, HG00186, NA19726, HG00274
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677004
Frequency
Sample Size1151
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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