A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050602



Internal ID19139821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6635558..6796980hg38UCSC Ensembl
Innerchr10:6677520..6838942hg19UCSC Ensembl
Innerchr10:6717526..6878948hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38161423
hg19161423
hg18161423
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv668n100
Supporting Variantsnssv3494608
Samples
Known GenesLINC00706, LINC00707
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050602
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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