A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970767



Internal ID18893964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:110002461..110002526hg38UCSC Ensembl
Outerchr10:111762219..111762284hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122556
Supporting Variants
SamplesKWS2
Known GenesADD3-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970767
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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