A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3994325



Internal ID18869640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:49964161..49965190hg38UCSC Ensembl
Outerchr10:51269900..51270800hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg381030
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143639
Supporting Variants
SamplesKWS1
Known GenesLOC728407, PARG
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3994325
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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