A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036128



Internal ID18778659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10404948..10470444hg38UCSC Ensembl
Innerchr16:10498805..10564301hg19UCSC Ensembl
Innerchr16:10406306..10471802hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3865497
hg1965497
hg1865497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557128
Samples
Known GenesATF7IP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036128
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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