A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121433



Internal ID19254785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10206601..10206772hg38UCSC Ensembl
OuterchrY:10044210..10044381hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4343n106
Supporting Variantsnssv3965433
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121433
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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