A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141182



Internal ID19269781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:125885831..125918431hg38UCSC Ensembl
Outerchr10:127574400..127607000hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3832601
hg1932601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv531n106
Supporting Variantsnssv3992689
SamplesKWS2
Known GenesFANK1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141182
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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