A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1130991



Internal ID18904869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:3084708..3086108hg38UCSC Ensembl
Outerchr10:3126900..3128300hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg381401
hg191401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv343n106
Supporting Variantsnssv3967697
SamplesKWS2
Known GenesPFKP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1130991
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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