A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997407



Internal ID17290359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:18401870..18402669hg38UCSC Ensembl
Outerchr6:18402101..18402900hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950135
Supporting Variants
SamplesBILGI_BIOE
Known GenesRNF144B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997407
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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