A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131007



Internal ID19271095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:124744031..124744931hg38UCSC Ensembl
Outerchr10:126432600..126433500hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967716
SamplesKWS2
Known GenesFAM53B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131007
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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