A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119009



Internal ID18911835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:74416783..74456583hg38UCSC Ensembl
Outerchr4:75282500..75322300hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3839801
hg1939801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2829n106
Supporting Variantsnssv3981803
SamplesKWS1
Known GenesAREG
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119009
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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