A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2829n106



Internal ID20162186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:74415583..74457483hg38UCSC Ensembl
chr4:75281300..75323200hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3841901
hg1941901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1119009, nsv1133586
SamplesKWS1, KWS2
Known GenesAREG
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2829n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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