A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957008



Internal ID16959195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:148375783..148379265hg38UCSC Ensembl
Outerchr7:148072875..148076357hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg383483
hg193483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000947
SamplesBILGI_BIOE
Known GenesCNTNAP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957008
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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