A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135629



Internal ID19259962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:183464253..183464319hg38UCSC Ensembl
Outerchr4:184385406..184385472hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2963n106
Supporting Variantsnssv3989191, nssv3968863
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135629
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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