A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957485



Internal ID19220206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:42021918..42022102hg38UCSC Ensembl
Outerchr4:42023935..42024119hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128057
Supporting Variants
SamplesKWS1
Known GenesSLC30A9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957485
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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