A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545106



Internal ID18843387
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 StatusS
Merged Variantsnsv1055193
Supporting Variants
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)nssv3545106
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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