A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3994853



Internal ID19221010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:135200..202200hg38UCSC Ensembl
Outerchr6:135200..202200hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3867001
hg1967001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1144130
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3994853
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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