A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151704



Internal ID18856719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:76165824..76171271hg38UCSC Ensembl
Outerchr10:77925582..77931029hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385448
hg195448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003127
SamplesKWB1
Known GenesC10orf11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151704
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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