A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525102



Internal ID15452395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1465161..1467727hg38UCSC Ensembl
Innerchr16:1515162..1517728hg19UCSC Ensembl
Innerchr16:1455163..1457729hg18UCSC Ensembl
Innerchr16:1455163..1457729hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382567
hg192567
hg182567
hg172567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701161
Samples
Known GenesCLCN7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525102
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