A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001788



Internal ID18744319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16864355..16934111hg38UCSC Ensembl
Innerchr1:17190850..17260606hg19UCSC Ensembl
Innerchr1:17063437..17133193hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3869757
hg1969757
hg1869757
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv105n100
Supporting Variantsnssv3478437, nssv3700164, nssv3463205, nssv3469631, nssv3700165, nssv3474060
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)nsv1001788
Frequency
Sample Size29084
Observed Gain2
Observed Loss4
Observed Complex0
Frequencyn/a


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