A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519565



Internal ID15446858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6834935..6859324hg38UCSC Ensembl
Innerchr4:6836662..6861051hg19UCSC Ensembl
Innerchr4:6887563..6911952hg18UCSC Ensembl
Innerchr4:6954734..6979123hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3824390
hg1924390
hg1824390
hg1724390
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656901, nssv676697, nssv703985, nssv672381
Samples
Known GenesKIAA0232
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519565
Frequency
Sample Size2026
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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