A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148009



Internal ID19198713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10206639..10206777hg38UCSC Ensembl
OuterchrY:10044248..10044386hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001518
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148009
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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