A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014725



Internal ID18757260
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 StatusM
Merged Variantsdgv360n100
Supporting Variantsnssv3486259, nssv3492900
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)nsv1014725
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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