A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986352



Internal ID18868022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:55403079..55403335hg38UCSC Ensembl
Outerchr4:56269246..56269502hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131801
Supporting Variants
SamplesKWS1
Known GenesTMEM165
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986352
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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