A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127113



Internal ID18919081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:59893741..59893804hg38UCSC Ensembl
Outerchr10:61653499..61653562hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985467
SamplesKWS1
Known GenesCCDC6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127113
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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