A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661207



Internal ID9580626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46373257..46397356hg38UCSC Ensembl
Outerchr10:46372885..46397726hg38UCSC Ensembl
Innerchr10:47744516..47768622hg19UCSC Ensembl
Outerchr10:47744145..47768992hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3824842
hg1924848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv135e199
Supporting Variantsessv5961165, essv5402541, essv5782902, essv5661305, essv6025534, essv6222589, essv5910623, essv5488554, essv6410997, essv5628535, essv6170458, essv5879948, essv6305543, essv5949203, essv5994073, essv6304340, essv6086320, essv6453377, essv6047991, essv5562360
SamplesNA19664, NA19777, NA19684, NA19728, NA19678, NA19723, NA19782, NA19720, NA19651, NA19719, NA19725, NA19717, NA19788, NA19750, NA19675, NA19679, NA19786, NA19783, NA19716, NA19676
Known GenesANXA8L1, ANXA8L2, FAM25B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661207
Frequency
Sample Size1151
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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