A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038656



Internal ID19127875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55950570..56009533hg38UCSC Ensembl
Innerchr10:57710330..57769294hg19UCSC Ensembl
Innerchr10:57380336..57439300hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3858964
hg1958965
hg1858965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv868n100
Supporting Variantsnssv3510306
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)nsv1038656
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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