A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520664



Internal ID15101271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46911729..46967279hg38UCSC Ensembl
Innerchr19:47414986..47470536hg19UCSC Ensembl
Innerchr19:52106826..52162376hg18UCSC Ensembl
Innerchr19:52106826..52162376hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3855551
hg1955551
hg1855551
hg1755551
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674747, nssv679226, nssv673709, nssv703982, nssv682492
Samples
Known GenesARHGAP35
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520664
Frequency
Sample Size2026
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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