A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4343n106



Internal ID22798171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10206601..10206779hg38UCSC Ensembl
chrY:10044210..10044388hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121433, nsv1114881, nsv1111766, nsv1128429
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4343n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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