A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111869



Internal ID18921313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:59681405..59681486hg38UCSC Ensembl
Outerchr10:61441163..61441244hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv462n106
Supporting Variantsnssv3982766, nssv3988977
SamplesKWS2, KWS1
Known GenesSLC16A9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111869
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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