A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003002



Internal ID18847209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:75558839..75559006hg38UCSC Ensembl
Outerchr17:73554920..73555087hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151582
Supporting Variants
SamplesKWB1
Known GenesLLGL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003002
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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