A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002108



Internal ID19091325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35882233..35924098hg38UCSC Ensembl
Innerchr4:35883855..35925720hg19UCSC Ensembl
Innerchr4:35560250..35602115hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3841866
hg1941866
hg1841866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625027
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)nsv1002108
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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