A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151604



Internal ID19199107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:41378547..41381548hg38UCSC Ensembl
Outerchr17:39534799..39537800hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg383002
hg193002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003027
SamplesKWB1
Known GenesKRT34
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151604
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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