A curated catalogue of human genomic structural variation
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Variant Details
Variant: nsv604415
Internal ID
16045138
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr6:104813138..104814114
hg38
UCSC
Ensembl
Inner
chr6:105261013..105261989
hg19
UCSC
Ensembl
Inner
chr6:105367706..105368682
hg18
UCSC
Ensembl
Cytoband
6q16.3
Allele length
Assembly
Allele length
hg38
977
hg19
977
hg18
977
Variant Type
CNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
dgv10891n54
Supporting Variants
nssv1071823
,
nssv1071826
,
nssv1071824
,
nssv1071820
,
nssv1071822
,
nssv1071827
,
nssv1071821
,
nssv1071819
,
nssv1071825
Samples
Known Genes
HACE1
Method
SNP array
Analysis
Illumina SNP array copy number analysis
Platform
Not reported
Comments
Reference
Cooper_et_al_2011
Pubmed ID
21841781
Accession Number(s)
nsv604415
Frequency
Sample Size
17421
Observed Gain
0
Observed Loss
9
Observed Complex
0
Frequency
n/a
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