A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122155



Internal ID18920091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:37291796..37293996hg38UCSC Ensembl
Outerchr7:37331400..37333600hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg382201
hg192201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969597
SamplesKWS2
Known GenesELMO1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122155
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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