A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112678



Internal ID19268178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:96528670..96533770hg38UCSC Ensembl
Outerchr15:97071900..97077000hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg385101
hg195101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967163
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112678
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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