A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700528



Internal ID15090494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162381712..162420947hg38UCSC Ensembl
Innerchr6:162802744..162841979hg19UCSC Ensembl
Innerchr6:162722734..162761969hg18UCSC Ensembl
Innerchr6:162773155..162812390hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3839236
hg1939236
hg1839236
hg1739236
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517562
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700528
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