A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001034



Internal ID18743565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16876990..16931137hg38UCSC Ensembl
Innerchr1:17203485..17257632hg19UCSC Ensembl
Innerchr1:17076072..17130219hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3854148
hg1954148
hg1854148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv115n100
Supporting Variantsnssv3473193, nssv3475107, nssv3478331, nssv3464310
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001034
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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