A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4000007



Internal ID19193873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10112190..10122391hg38UCSC Ensembl
OuterchrY:9949799..9960000hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3810202
hg1910202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1147235
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4000007
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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