A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056780



Internal ID19145999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19591492..19634157hg38UCSC Ensembl
Innerchr17:19494805..19537470hg19UCSC Ensembl
Innerchr17:19435397..19478062hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3842666
hg1942666
hg1842666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3117n100
Supporting Variantsnssv3560543, nssv3560542
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)nsv1056780
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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