A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990461



Internal ID18898210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:74212832..74212896hg38UCSC Ensembl
Outerchr10:75972590..75972654hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113313
Supporting Variants
SamplesKWS2
Known GenesADK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990461
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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