A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515798



Internal ID15442855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29068198..29146274hg38UCSC Ensembl
Innerchr15:29360401..29438477hg19UCSC Ensembl
Innerchr15:27147693..27225769hg18UCSC Ensembl
Innerchr15:27147693..27225769hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3878077
hg1978077
hg1878077
hg1778077
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697106, nssv676232, nssv669148, nssv685533, nssv679219, nssv677652, nssv682130, nssv673335, nssv655233, nssv691870, nssv699590, nssv657071, nssv674435, nssv657133, nssv688880, nssv697105, nssv685482, nssv655522, nssv680856, nssv674745, nssv664819, nssv677504, nssv667940, nssv685637, nssv676848, nssv667283, nssv689214
Samples
Known GenesAPBA2, FAM189A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515798
Frequency
Sample Size2026
Observed Gain2
Observed Loss25
Observed Complex0
Frequencyn/a


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