A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3992621



Internal ID19227124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:13467577..13467639hg38UCSC Ensembl
OuterchrY:15579457..15579519hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141114
Supporting Variants
SamplesKWS2
Known GenesUTY
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3992621
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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