A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145488



Internal ID19279900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:124404402..124404489hg38UCSC Ensembl
Outerchr10:126092971..126093058hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv530n106
Supporting Variantsnssv3983114
SamplesKWS1
Known GenesOAT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145488
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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