A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963481



Internal ID19218318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:115952105..115952491hg38UCSC Ensembl
Outerchr10:117711616..117712002hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111373
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963481
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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