A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990442



Internal ID18892504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:52156164..52156216hg38UCSC Ensembl
Outerchr10:53915924..53915976hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137921
Supporting Variants
SamplesKWS2
Known GenesPRKG1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990442
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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