A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137875



Internal ID18928405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:12625147..12625220hg38UCSC Ensembl
Outerchr10:12667146..12667219hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990398
SamplesKWS2
Known GenesCAMK1D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137875
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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