A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054652



Internal ID19143871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56568747..56725241hg38UCSC Ensembl
Innerchr10:58328507..58485001hg19UCSC Ensembl
Innerchr10:57998513..58155007hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38156495
hg19156495
hg18156495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv869n100
Supporting Variantsnssv3511050, nssv3511222, nssv3512793, nssv3519466, nssv3507655, nssv3507819
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054652
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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