A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515709



Internal ID15096316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:87941544..87953014hg38UCSC Ensembl
Innerchr14:88407888..88419358hg19UCSC Ensembl
Innerchr14:87477641..87489111hg18UCSC Ensembl
Innerchr14:87477641..87489111hg17UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3811471
hg1911471
hg1811471
hg1711471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv667594, nssv662713, nssv664498, nssv681890
Samples
Known GenesGALC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515709
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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