A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516032



Internal ID15096639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3569622..3571219hg38UCSC Ensembl
Innerchr18:3569620..3571217hg19UCSC Ensembl
Innerchr18:3559620..3561217hg18UCSC Ensembl
Innerchr18:3559620..3561217hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381598
hg191598
hg181598
hg171598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705273, nssv685180, nssv672483, nssv685758, nssv693761, nssv675856, nssv679141, nssv667318, nssv691554, nssv666453, nssv665823, nssv654777, nssv682463, nssv693512
Samples
Known GenesDLGAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516032
Frequency
Sample Size2026
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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