A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718218



Internal ID19016499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97347844..97393999hg38UCSC Ensembl
Innerchr15:97891074..97937229hg19UCSC Ensembl
Innerchr15:95692078..95738233hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3846156
hg1946156
hg1846156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051209
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718218
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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