A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055193



Internal ID19144412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41354648..41370910hg38UCSC Ensembl
Innerchr17:39510900..39527162hg19UCSC Ensembl
Innerchr17:36764426..36780688hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3816263
hg1916263
hg1816263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3173n100
Supporting Variantsnssv3545106
Samples
Known GenesKRT33B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055193
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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