A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726646



Internal ID18678241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56197884..56229646hg38UCSC Ensembl
Innerchr19:56709253..56741015hg19UCSC Ensembl
Innerchr19:61401065..61432827hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3831763
hg1931763
hg1831763
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065286
Supporting Variants
Samples
Known GenesZSCAN5A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726646
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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