A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986577



Internal ID18863013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:36604450..36605899hg38UCSC Ensembl
Outerchr6:36572227..36573676hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381450
hg191450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131956
Supporting Variants
SamplesKWS1
Known GenesSRSF3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986577
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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