A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997442



Internal ID16943708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:43275063..43310262hg38UCSC Ensembl
Outerchr6:43242801..43278000hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3835200
hg1935200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950170
Supporting Variants
SamplesBILGI_BIOE
Known GenesCRIP3, SLC22A7, TTBK1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997442
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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