A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987634



Internal ID18861458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:61915292..61915351hg38UCSC Ensembl
Outerchr10:63675051..63675110hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132841
Supporting Variants
SamplesKWS1
Known GenesARID5B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987634
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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