A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703593



Internal ID15093559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:109911223..109952819hg38UCSC Ensembl
Innerchr9:112673503..112715099hg19UCSC Ensembl
Innerchr9:111713324..111754920hg18UCSC Ensembl
Innerchr9:109753058..109794654hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3841597
hg1941597
hg1841597
hg1741597
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527195
Supporting Variants
Samples
Known GenesPALM2, PALM2-AKAP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703593
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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