A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150152



Internal ID18852832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:15229747..15229846hg38UCSC Ensembl
Outerchr10:15271746..15271845hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003452
SamplesKWB1
Known GenesFAM171A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150152
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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