A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055237



Internal ID18797768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46114400..46169798hg38UCSC Ensembl
Innerchr17:44191766..44247164hg19UCSC Ensembl
Innerchr17:41547543..41602941hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3855399
hg1955399
hg1855399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3205n100
Supporting Variantsnssv3720617
Samples
Known GenesKANSL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055237
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer