A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515627



Internal ID15096234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100928605..100947769hg38UCSC Ensembl
Innerchr10:102688362..102707526hg19UCSC Ensembl
Innerchr10:102678352..102697516hg18UCSC Ensembl
Innerchr10:102678352..102697516hg17UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3819165
hg1919165
hg1819165
hg1719165
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686756, nssv678267, nssv664153, nssv676676, nssv669368, nssv685656, nssv674074, nssv681366, nssv669143, nssv669086, nssv680693, nssv661591
Samples
Known GenesFAM178A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515627
Frequency
Sample Size2026
Observed Gain10
Observed Loss2
Observed Complex0
Frequencyn/a


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