A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129895



Internal ID18938370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:112398023..112398388hg38UCSC Ensembl
Outerchr10:114157781..114158146hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv517n106
Supporting Variantsnssv3965032
SamplesKWS2
Known GenesACSL5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129895
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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