A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515607



Internal ID15443218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:87693597..87717585hg38UCSC Ensembl
Innerchr3:87742747..87766735hg19UCSC Ensembl
Innerchr3:87825437..87849425hg18UCSC Ensembl
Innerchr3:87825437..87849425hg17UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg3823989
hg1923989
hg1823989
hg1723989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686469, nssv664067, nssv678419, nssv677901, nssv655430
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515607
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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