A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143621



Internal ID19267412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:11611201..11611801hg38UCSC Ensembl
Outerchr10:11653200..11653800hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv364n106
Supporting Variantsnssv3994306
SamplesKWS1
Known GenesUSP6NL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143621
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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