A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003564



Internal ID18840481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:94773960..94774238hg38UCSC Ensembl
Outerchr10:47088420..47088698hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150265
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003564
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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