A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057837



Internal ID19147056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:263243..314233hg38UCSC Ensembl
Innerchr17:113034..164024hg19UCSC Ensembl
Innerchr17:113034..164024hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3850991
hg1950991
hg1850991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560036
Samples
Known GenesRPH3AL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057837
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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