A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139280



Internal ID18923583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87110985..87111317hg38UCSC Ensembl
Outerchr4:88032137..88032469hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2846n106
Supporting Variantsnssv3973976, nssv3970465
SamplesKWS2, KWS1
Known GenesAFF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139280
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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