A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971902



Internal ID18260433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13229614..13234697hg38UCSC Ensembl
Innerchr10:13271614..13276697hg19UCSC Ensembl
Innerchr10:13311620..13316703hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg385084
hg195084
hg185084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758744
SamplesHGDP00542
Known GenesUCMA
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971902
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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