A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013150



Internal ID19102368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94665950..94687251hg38UCSC Ensembl
Innerchr1:95131506..95152807hg19UCSC Ensembl
Innerchr1:94904094..94925395hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3821302
hg1921302
hg1821302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv208n100
Supporting Variantsnssv3474654
Samples
Known GenesLINC01057
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013150
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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