A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683845



Internal ID15420497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101328323..101494033hg38UCSC Ensembl
Innerchr7:100971604..101137314hg19UCSC Ensembl
Innerchr7:100758324..100924034hg18UCSC Ensembl
Innerchr7:100565039..100730749hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38165711
hg19165711
hg18165711
hg17165711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517175
Supporting Variants
Samples
Known GenesCOL26A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683845
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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