A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055884



Internal ID19145103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:57210510..57226803hg38UCSC Ensembl
Innerchr17:55287871..55304164hg19UCSC Ensembl
Innerchr17:52642870..52659163hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3816294
hg1916294
hg1816294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3269n100
Supporting Variantsnssv3567700
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)nsv1055884
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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