A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515519



Internal ID15096126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69476497..69504046hg38UCSC Ensembl
Innerchr9:72091413..72118962hg19UCSC Ensembl
Innerchr9:71281233..71308782hg18UCSC Ensembl
Innerchr9:69320967..69348516hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3827550
hg1927550
hg1827550
hg1727550
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv655439, nssv664193, nssv693526, nssv655725, nssv661864, nssv671411, nssv677635, nssv666088, nssv651809, nssv678641, nssv686124, nssv672478, nssv681182, nssv691788, nssv657632, nssv658314, nssv679148
Samples
Known GenesAPBA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515519
Frequency
Sample Size2026
Observed Gain5
Observed Loss12
Observed Complex0
Frequencyn/a


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