A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000224



Internal ID17293176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:2688707..2711506hg38UCSC Ensembl
Outerchr17:2592001..2614800hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3822800
hg1922800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952105
Supporting Variants
SamplesBILGI_BIOE
Known GenesCLUH, MIR6776
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000224
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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