A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3486259



Internal ID18727214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:148916177..149361265hg19UCSC Ensembl
Innerchr1:147182801..147627889hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg19445089
hg18445089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014725
Supporting Variants
Samples
Known GenesLOC101929780, LOC388692, LOC645166, NBPF23
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3486259
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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