A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970729



Internal ID18899790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:49069970..49070287hg38UCSC Ensembl
Outerchr10:50278015..50278332hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122526
Supporting Variants
SamplesKWS2
Known GenesVSTM4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970729
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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