A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119133



Internal ID19250709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:98400188..98401088hg38UCSC Ensembl
Outerchr7:98029500..98030400hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981938
SamplesKWS1
Known GenesBAIAP2L1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119133
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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