A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702402



Internal ID15092368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56127476..56148373hg38UCSC Ensembl
Innerchr19:56638845..56659742hg19UCSC Ensembl
Innerchr19:61330657..61351554hg18UCSC Ensembl
Innerchr19:61330657..61351554hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3820898
hg1920898
hg1820898
hg1720898
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517365
Supporting Variants
Samples
Known GenesZNF444
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702402
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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