A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128429



Internal ID19261506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10206634..10206775hg38UCSC Ensembl
OuterchrY:10044243..10044384hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4343n106
Supporting Variantsnssv3958777
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128429
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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