A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965932



Internal ID18896953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:52224506..52274175hg38UCSC Ensembl
Outerchr10:53984266..54033935hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3849670
hg1949670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112235
Supporting Variants
SamplesKWS2
Known GenesPRKG1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965932
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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