A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982766



Internal ID18876226
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 StatusS
Merged Variantsnsv1111869
Supporting Variants
SamplesKWS1
Known GenesSLC16A9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982766
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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