A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131636



Internal ID18919768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:44927747..44928699hg38UCSC Ensembl
Outerchr10:45423195..45424147hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38953
hg19953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv438n106
Supporting Variantsnssv3986114
SamplesKWS1
Known GenesTMEM72, TMEM72-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131636
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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