A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132095



Internal ID18904071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:147657960..147658273hg38UCSC Ensembl
Outerchr7:147355052..147355365hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986772
SamplesKWS1
Known GenesCNTNAP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132095
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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