A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832171



Internal ID15779441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:87941544..87953014hg38UCSC Ensembl
Innerchr14:88407888..88419358hg19UCSC Ensembl
Innerchr14:87477641..87489111hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3811471
hg1911471
hg1811471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565511
Supporting Variants
Samples
Known GenesGALC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv832171
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer