A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997783



Internal ID19157320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:22221880..22336920hg38UCSC Ensembl
Innerchr4:22223503..22338543hg19UCSC Ensembl
Innerchr4:21832601..21947641hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38115041
hg19115041
hg18115041
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620580
Samples
Known GenesLOC100505912
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997783
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