A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988992



Internal ID18889191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3217508..3222856hg38UCSC Ensembl
Outerchr11:3238738..3244086hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385349
hg195349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135426
Supporting Variants
SamplesKWS2
Known GenesMRGPRG, MRGPRG-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988992
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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