A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007255



Internal ID18749786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15330646..15352345hg38UCSC Ensembl
Innerchr1:15657142..15678841hg19UCSC Ensembl
Innerchr1:15529729..15551428hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3821700
hg1921700
hg1821700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3475158
Samples
Known GenesFHAD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007255
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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