A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726645



Internal ID18678240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56044576..56208893hg38UCSC Ensembl
Innerchr19:56555942..56720262hg19UCSC Ensembl
Innerchr19:61247754..61412074hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38164318
hg19164321
hg18164321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057820
Supporting Variants
Samples
Known GenesGALP, NLRP5, ZNF444, ZNF787, ZSCAN5B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726645
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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