A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670000



Internal ID15059966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21638256..22743028hg38UCSC Ensembl
Innerchr17:21539613..22242355hg19UCSC Ensembl
Innerchr17:21480206..22166482hg18UCSC Ensembl
Innerchr17:21480206..22166482hg17UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg381104773
hg19702743
hg18686277
hg17686277
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516664
Supporting Variants
Samples
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670000
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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