A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113313



Internal ID18910304
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 StatusM
Merged Variants
Supporting Variantsnssv3982779, nssv3990461
SamplesKWS1, KWS2
Known GenesADK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113313
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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