A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771228



Internal ID19312008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7751824..7752078hg38UCSC Ensembl
chr10:7793787..7794041hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072672
Supporting Variants
SamplesKWP1
Known GenesKIN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771228
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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