A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138887



Internal ID18915775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:207095347..207112164hg38UCSC Ensembl
Outerchr2:207960071..207976888hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3816818
hg1916818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991496
SamplesKWS2
Known GenesKLF7, MIR2355
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138887
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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