A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132092



Internal ID18930649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:146602875..146605550hg38UCSC Ensembl
Outerchr7:146299967..146302642hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg382676
hg192676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986769
SamplesKWS1
Known GenesCNTNAP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132092
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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