A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762637



Internal ID19307016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1592206..1610407hg38UCSC Ensembl
chrY:1661099..1679300hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3818202
hg1918202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078146
Supporting Variants
SamplesKWP1
Known GenesAKAP17A, ASMT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762637
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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