A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997126



Internal ID18843764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46262863..46366783hg38UCSC Ensembl
Outerchr10:47634099..47738000hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38103921
hg19103902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145763
Supporting Variants
SamplesKWB1
Known GenesANTXRL, ANTXRLP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997126
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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