A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947429



Internal ID18247591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:61970878..61985935hg38UCSC Ensembl
Innerchr1:62436550..62451607hg19UCSC Ensembl
Innerchr1:62209138..62224195hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3815058
hg1915058
hg1815058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2765874
SamplesHGDP01284
Known GenesINADL
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947429
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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