A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675699



Internal ID15065665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34480941..34505360hg38UCSC Ensembl
Innerchr19:34971846..34996265hg19UCSC Ensembl
Innerchr19:39663686..39688105hg18UCSC Ensembl
Innerchr19:39663686..39688105hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3824420
hg1924420
hg1824420
hg1724420
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517392
Supporting Variants
Samples
Known GenesWTIP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv675699
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