A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061415



Internal ID19150634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:57210510..57230319hg38UCSC Ensembl
Innerchr17:55287871..55307680hg19UCSC Ensembl
Innerchr17:52642870..52662679hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3819810
hg1919810
hg1819810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3269n100
Supporting Variantsnssv3567701
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061415
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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