A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055973



Internal ID19145192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35334296..35422683hg38UCSC Ensembl
Innerchr16:34568667..34657054hg19UCSC Ensembl
Innerchr16:34426168..34514555hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg3888388
hg1988388
hg1888388
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2969n100
Supporting Variantsnssv3722678, nssv3559149
Samples
Known GenesLOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055973
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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