A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517343



Internal ID15444636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:807215..1386951hg38UCSC Ensembl
Innerchr3:848898..1428635hg19UCSC Ensembl
Innerchr3:823898..1403635hg18UCSC Ensembl
Innerchr3:823898..1403635hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38579737
hg19579738
hg18579738
hg17579738
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664739, nssv660938, nssv693695, nssv687451, nssv680980, nssv675641, nssv675545, nssv702191, nssv653211, nssv672083, nssv674906, nssv693169, nssv704994, nssv678732, nssv675797, nssv705320, nssv674568, nssv671856, nssv695189, nssv684338, nssv657747, nssv677924, nssv662329, nssv697376, nssv676753
Samples
Known GenesCNTN6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517343
Frequency
Sample Size2026
Observed Gain3
Observed Loss31
Observed Complex0
Frequencyn/a


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