A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951012



Internal ID16953199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:64709329..64727728hg38UCSC Ensembl
Outerchr11:64476801..64495200hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3818400
hg1918400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999560
SamplesBILGI_BIOE
Known GenesNRXN2, RASGRP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951012
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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