A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695297



Internal ID15431949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149332656..149336982hg38UCSC Ensembl
Innerchr6:149653792..149658118hg19UCSC Ensembl
Innerchr6:149695485..149699811hg18UCSC Ensembl
Innerchr6:149695485..149699811hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg384327
hg194327
hg184327
hg174327
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517889
Supporting Variants
Samples
Known GenesTAB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695297
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