A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999580



Internal ID19159117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94665110..94690029hg38UCSC Ensembl
Innerchr1:95130666..95155585hg19UCSC Ensembl
Innerchr1:94903254..94928173hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3824920
hg1924920
hg1824920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv208n100
Supporting Variantsnssv3463494, nssv3481830, nssv3474960, nssv3478830, nssv3478107
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)nsv999580
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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