A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684164



Internal ID15420816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56687157..56699418hg38UCSC Ensembl
Innerchr19:57198525..57210786hg19UCSC Ensembl
Innerchr19:61890337..61902598hg18UCSC Ensembl
Innerchr19:61890337..61902598hg17UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3812262
hg1912262
hg1812262
hg1712262
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517449
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684164
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