A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010903



Internal ID18753436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103940741..104926319hg38UCSC Ensembl
Innerchr1:104483363..105468941hg19UCSC Ensembl
Innerchr1:104284886..105270464hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38985579
hg19985579
hg18985579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3493364
Samples
Known GenesLOC100129138, MIR548H3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010903
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