A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700903



Internal ID15090869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7141418..8338431hg38UCSC Ensembl
Innerchr9:7141418..8338431hg19UCSC Ensembl
Innerchr9:7131418..8328431hg18UCSC Ensembl
Innerchr9:7131418..8328431hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381197014
hg191197014
hg181197014
hg171197014
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524896
Supporting Variants
Samples
Known GenesKDM4C, PTPRD, TMEM261
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700903
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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