A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001381



Internal ID19090598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:5051997..5113945hg38UCSC Ensembl
Innerchr1:5112057..5174005hg19UCSC Ensembl
Innerchr1:5011917..5073865hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3861949
hg1961949
hg1861949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696762, nssv3479297, nssv3480432, nssv3472304, nssv3465441, nssv3468116
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001381
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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