A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062102



Internal ID19151321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6197711..6229480hg38UCSC Ensembl
Innerchr17:6101031..6132800hg19UCSC Ensembl
Innerchr17:6041755..6073524hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3831770
hg1931770
hg1831770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3090n100
Supporting Variantsnssv3560140, nssv3560141, nssv3560142
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)nsv1062102
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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