A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1130197



Internal ID19252731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:58292540..58328940hg38UCSC Ensembl
Outerchr10:60052300..60088700hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3836401
hg1936401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv460n106
Supporting Variantsnssv3966109
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1130197
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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