A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980496



Internal ID18615696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:127457287..127470038hg38UCSC Ensembl
Innerchr4:128378442..128391193hg19UCSC Ensembl
Innerchr4:128597892..128610643hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg3812752
hg1912752
hg1812752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2757893
SamplesHGDP01029
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv980496
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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