A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966695



Internal ID19226026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97849343..97850443hg38UCSC Ensembl
Outerchr10:99609100..99610200hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112594
Supporting Variants
SamplesKWS2
Known GenesGOLGA7B, LINC00866
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966695
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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