A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137952



Internal ID18939540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:99814523..99814581hg38UCSC Ensembl
Outerchr10:101574280..101574338hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv506n106
Supporting Variantsnssv3990476
SamplesKWS2
Known GenesABCC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137952
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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