A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2846n106



Internal ID20162203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87110985..87111317hg38UCSC Ensembl
chr4:88032137..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 Variants
Supporting Variantsnsv1139280, nsv1120017
SamplesKWS1, KWS2
Known GenesAFF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2846n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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