A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677534



Internal ID15067500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:95661806..96017630hg38UCSC Ensembl
Innerchr2:96327554..96683378hg19UCSC Ensembl
Innerchr2:95691281..96047105hg18UCSC Ensembl
Innerchr2:95749428..96105252hg17UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38355825
hg19355825
hg18355825
hg17355825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516044
Supporting Variants
Samples
Known GenesFAHD2CP, LINC00342
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677534
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